Release v2021-04-07 · monarch-initiative/mondo

New Classes

MONDO:0025353 developmental and epileptic encephalopathy, 90
MONDO:0025354 spermatogenic failure, X-linked, 3
MONDO:0030894 AMED syndrome, digenic
MONDO:0030895 nephrotic syndrome, type 22
MONDO:0030898 immunodeficiency 76
MONDO:0030899 oculocutaneous albinism, type 8
MONDO:0030902 mitochondrial complex 1 deficiency, nuclear type 36
MONDO:0030903 Hermansky-Pudlak syndrome 11
MONDO:0030905 deafness, autosomal recessive 117
MONDO:0030924 proteasome-associated autoinflammatory syndrome 5
MONDO:0030925 oocyte maturation defect 10
MONDO:0030926 spermatogenic failure 51
MONDO:0030927 myofibrillar myopathy 11
MONDO:0030928 microcephaly 26, primary, autosomal dominant
MONDO:0030929 microcephaly 27, primary, autosomal dominant
MONDO:0030931 proteasome-associated autoinflammatory syndrome 4
MONDO:0030933 Joubert syndrome 37
MONDO:0030934 intellectual developmental disorder, autosomal dominant 64
MONDO:0030935 mitochondrial complex 2 deficiency, nuclear type 2
MONDO:0030936 epilepsy, progressive myoclonic, 12
MONDO:0030937 mitochondrial complex 2 deficiency, nuclear type 3
MONDO:0030938 spermatogenic failure 52
MONDO:0030939 premature ovarian failure 18
MONDO:0030941 erythrokeratodermia variabilis et progressiva 7
MONDO:0030953 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2
MONDO:0030961 Olmsted syndrome 2
MONDO:0031230 mitochondrial complex II deficiency, nuclear type
MONDO:0031421 Olmsted syndrome
MONDO:0031439 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
MONDO:0100290 colon serrated polyposis
MONDO:0100291 early T cell progenitor acute lymphoblastic leukemia
MONDO:0100294 mitochondrial complex II deficiency, nuclear type 1
MONDO:0100296 Olmsted syndrome 1
MONDO:0100297 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1
MONDO:0100316 long QT syndrome 1
+id: disease_has_infectious_agent ! disease has infectious agent

Obsoletions

MONDO:0000606 gluten allergy --> obsolete gluten allergy
MONDO:0000772 pollen allergy --> obsolete pollen allergy
MONDO:0000773 Timothy grass allergy --> obsolete Timothy grass allergy
MONDO:0000776 metal allergy --> obsolete metal allergy
MONDO:0000779 apple allergy --> obsolete apple allergy
MONDO:0000780 apricot allergy --> obsolete apricot allergy
MONDO:0000785 peach allergy --> obsolete peach allergy
MONDO:0000786 plum allergy --> obsolete plum allergy
MONDO:0000787 tomato allergy --> obsolete tomato allergy
MONDO:0000788 fish allergy --> obsolete fish allergy
MONDO:0000789 Atlantic cod allergy --> obsolete Atlantic cod allergy
MONDO:0000790 Atlantic salmon allergy --> obsolete Atlantic salmon allergy
MONDO:0000791 carp allergy --> obsolete carp allergy
MONDO:0000793 rainbow trout allergy --> obsolete rainbow trout allergy
MONDO:0000794 beta-lactam allergy --> obsolete beta-lactam allergy
MONDO:0000795 penicillin allergy --> obsolete penicillin allergy
MONDO:0000796 cow milk allergy (disease) --> obsolete cow milk allergy (disease)
MONDO:0000797 goat milk allergy --> obsolete goat milk allergy
MONDO:0000798 mollusc allergy --> obsolete mollusc allergy
MONDO:0000799 crustacean allergy --> obsolete crustacean allergy
MONDO:0000800 brown shrimp allergy --> obsolete brown shrimp allergy
MONDO:0000801 green mud crab allergy --> obsolete green mud crab allergy
MONDO:0000802 Indian prawn allergy --> obsolete Indian prawn allergy
MONDO:0000803 tiger prawn allergy --> obsolete tiger prawn allergy
MONDO:0000804 white shrimp allergy --> obsolete white shrimp allergy
MONDO:0000805 snail allergy --> obsolete snail allergy
MONDO:0000806 horned turban snail allergy --> obsolete horned turban snail allergy
MONDO:0000865 congenital fiber-type disproportion --> obsolete congenital fiber-type disproportion
MONDO:0000991 left bundle branch block --> obsolete left bundle branch block
MONDO:0001662 right bundle branch block (disease) --> obsolete right bundle branch block (disease)
MONDO:0002497 food allergy --> obsolete food allergy
MONDO:0005741 egg allergy --> obsolete egg allergy
MONDO:0006772 glycogen storage disease VIII --> obsolete glycogen storage disease VIII
MONDO:0006872 nut allergic reaction --> obsolete nut allergic reaction
MONDO:0007021 wheat allergic disease --> obsolete wheat allergic disease
MONDO:0007954 May-Hegglin anomaly --> obsolete May-Hegglin anomaly
MONDO:0008032 autosomal dominant limb-girdle muscular dystrophy type 1A --> obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
MONDO:0008646 long QT syndrome 1 --> obsolete long QT syndrome 1
MONDO:0009317 nonphotosensitive trichothiodystrophy --> obsolete nonphotosensitive trichothiodystrophy
MONDO:0009641 mitochondrial complex II deficiency --> obsolete mitochondrial complex II deficiency
MONDO:0009739 infantile neuroaxonal dystrophy --> obsolete infantile neuroaxonal dystrophy
MONDO:0010086 sudden infant death syndrome --> obsolete sudden infant death syndrome
MONDO:0012632 Alzheimer disease 15 --> obsolete Alzheimer disease 15
MONDO:0015147 other syndrome with lissencephaly as a major feature --> obsolete other syndrome with lissencephaly as a major feature
MONDO:0015226 syndrome with limb malformations as a major feature --> obsolete syndrome with limb malformations as a major feature
MONDO:0015319 rare disease with Pierre Robin syndrome --> obsolete rare disease with Pierre Robin syndrome
MONDO:0015332 rare developmental defect with connective tissue involvement --> obsolete rare developmental defect with connective tissue involvement
MONDO:0015475 rare head and neck malformation --> obsolete rare head and neck malformation
MONDO:0015506 rare syndrome with cardiac malformations --> obsolete rare syndrome with cardiac malformations
MONDO:0015603 rare odontal or periodontal disorder --> obsolete rare odontal or periodontal disorder
MONDO:0015652 chromosomal anomaly with epilepsy as a major feature --> obsolete chromosomal anomaly with epilepsy as a major feature
MONDO:0015662 hemorrhagic disorder due to an acquired coagulation factor defect --> obsolete hemorrhagic disorder due to an acquired coagulation factor defect
MONDO:0015669 rare disease with dentinogenesis imperfecta --> obsolete rare disease with dentinogenesis imperfecta
MONDO:0015847 rare vaginal malformation --> obsolete rare vaginal malformation
MONDO:0015851 rare breast malformation --> obsolete rare breast malformation
MONDO:0015857 rare non-malformative gynecologic or obstetric disease --> obsolete rare non-malformative gynecologic or obstetric disease
MONDO:0015858 rare non-malformative breast disease --> obsolete rare non-malformative breast disease
MONDO:0015859 rare non-malformative uterovaginal or vulvovaginal disease --> obsolete rare non-malformative uterovaginal or vulvovaginal disease
MONDO:0015861 rare uterine adnexal tumor --> obsolete rare uterine adnexal tumor
MONDO:0015875 rare non-malformative uterine adnexal disease --> obsolete rare non-malformative uterine adnexal disease
MONDO:0015876 rare vulvovaginal tumor --> obsolete rare vulvovaginal tumor
MONDO:0015885 rare insulin-resistance syndrome --> obsolete rare insulin-resistance syndrome
MONDO:0015887 rare diabetes mellitus type 2 --> obsolete rare diabetes mellitus type 2
MONDO:0015888 other rare diabetes mellitus --> obsolete other rare diabetes mellitus
MONDO:0015889 rare hypothalamic or pituitary disease --> obsolete rare hypothalamic or pituitary disease
MONDO:0015890 rare disorder with congenital hypogonadotropic hypogonadism --> obsolete rare disorder with congenital hypogonadotropic hypogonadism
MONDO:0015913 rare thrombotic disease of hematologic origin --> obsolete rare thrombotic disease of hematologic origin
MONDO:0015916 rare neuroinflammatory or neuroimmunological disease --> obsolete rare neuroinflammatory or neuroimmunological disease
MONDO:0015937 rare inflammatory eye disease --> obsolete rare inflammatory eye disease
MONDO:0015964 obsolete rare genetic palpebral, lacrimal system and conjunctival disease --> obsolete obsolete rare genetic palpebral, lacrimal system and conjunctival disease
MONDO:0015965 rare genetic refraction anomaly --> obsolete rare genetic refraction anomaly
MONDO:0015968 rare genetic hypothalamic or pituitary disease --> obsolete rare genetic hypothalamic or pituitary disease
MONDO:0015970 rare genetic parathyroid disease and phosphocalcic metabolism disorder --> obsolete rare genetic parathyroid disease and phosphocalcic metabolism disorder
MONDO:0016055 syndrome with corpus callosum agenesis /dysgenesis as a major feature --> obsolete syndrome with corpus callosum agenesis /dysgenesis as a major feature
MONDO:0016132 rare hereditary disease with peripheral neuropathy --> obsolete rare hereditary disease with peripheral neuropathy
MONDO:0016133 rare hereditary metabolic disease with peripheral neuropathy --> obsolete rare hereditary metabolic disease with peripheral neuropathy
MONDO:0016134 rare hereditary systemic disease with peripheral neuropathy --> obsolete rare hereditary systemic disease with peripheral neuropathy
MONDO:0016135 rare hereditary neurologic disease with peripheral neuropathy --> obsolete rare hereditary neurologic disease with peripheral neuropathy
MONDO:0016232 rare venous malformation --> obsolete rare venous malformation
MONDO:0016233 rare lymphatic system malformation --> obsolete rare lymphatic system malformation
MONDO:0016320 rare hereditary thrombophilia --> obsolete rare hereditary thrombophilia
MONDO:0016406 other metabolic disease with epilepsy --> obsolete other metabolic disease with epilepsy
MONDO:0016507 rare surgically correctable form of primary aldosteronism --> obsolete rare surgically correctable form of primary aldosteronism
MONDO:0016508 rare non surgically correctable form of primary aldosteronism --> obsolete rare non surgically correctable form of primary aldosteronism
MONDO:0016631 hemorrhagic disorder due to an acquired platelet anomaly --> obsolete hemorrhagic disorder due to an acquired platelet anomaly
MONDO:0016633 thrombotic disorder due to a constitutional coagulation factors defect --> obsolete thrombotic disorder due to a constitutional coagulation factors defect
MONDO:0016634 thrombotic disorder due to an acquired coagulation factors defect --> obsolete thrombotic disorder due to an acquired coagulation factors defect
MONDO:0016636 thrombotic disorder due to a constitutional platelet anomaly --> obsolete thrombotic disorder due to a constitutional platelet anomaly
MONDO:0016637 thrombotic disorder due to an acquired platelet anomaly --> obsolete thrombotic disorder due to an acquired platelet anomaly
MONDO:0016768 rare mucosal lichen planus --> obsolete rare mucosal lichen planus
MONDO:0016992 peeling skin syndrome type B --> obsolete peeling skin syndrome type B
MONDO:0017120 other syndrome with a central nervous system malformation as major feature --> obsolete other syndrome with a central nervous system malformation as major feature
MONDO:0017122 genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature --> obsolete genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
MONDO:0017125 oculofaciocardiodental syndrome --> obsolete oculofaciocardiodental syndrome
MONDO:0017142 hemorrhagic disorder due to a qualitative platelet defect --> obsolete hemorrhagic disorder due to a qualitative platelet defect
MONDO:0017159 syndrome with pulmonary hypertension as a major feature --> obsolete syndrome with pulmonary hypertension as a major feature
MONDO:0017166 rare tumor of salivary glands --> obsolete rare tumor of salivary glands
MONDO:0017631 rare tumor of gallbladder and extrahepatic biliary tract --> obsolete rare tumor of gallbladder and extrahepatic biliary tract
MONDO:0017633 rare intoxication due to medical products --> obsolete rare intoxication due to medical products
MONDO:0017637 rare parkinsonian syndrome due to intoxication --> obsolete rare parkinsonian syndrome due to intoxication
MONDO:0017652 rare disease with myoclonus as a major feature --> obsolete rare disease with myoclonus as a major feature
MONDO:0017657 rare paroxysmal movement disorder --> obsolete rare paroxysmal movement disorder
MONDO:0017661 rare parkinsonian syndrome due to genetic neurodegenerative disease --> obsolete rare parkinsonian syndrome due to genetic neurodegenerative disease
MONDO:0017665 rare genetic disease with myoclonus as a major feature --> obsolete rare genetic disease with myoclonus as a major feature
MONDO:0017669 disease with diffuse palmoplantar keratoderma as a major feature --> obsolete disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0017671 autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature --> obsolete autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0017674 disease with focal palmoplantar keratoderma as a major feature --> obsolete disease with focal palmoplantar keratoderma as a major feature
MONDO:0017678 obsolete disease with punctate palmoplantar keratoderma as a major feature --> obsolete obsolete disease with punctate palmoplantar keratoderma as a major feature
MONDO:0017679 obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature --> obsolete obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
MONDO:0017820 obsolete disease with Cushing syndrome as a major feature --> obsolete obsolete disease with Cushing syndrome as a major feature
MONDO:0018033 other immunodeficiency syndromes due to defects in innate immunity --> obsolete other immunodeficiency syndromes due to defects in innate immunity
MONDO:0018041 other immunodeficiency syndrome with predominantly antibody defects --> obsolete other immunodeficiency syndrome with predominantly antibody defects
MONDO:0018235 dysostosis with limb anomaly as a major feature --> obsolete dysostosis with limb anomaly as a major feature
MONDO:0018236 dysostosis with limb and face anomalies as a major feature --> obsolete dysostosis with limb and face anomalies as a major feature
MONDO:0018265 rare disorder with dystonia and other neurologic or systemic manifestation --> obsolete rare disorder with dystonia and other neurologic or systemic manifestation
MONDO:0018285 X-linked congenital disorder of glycosylation with intellectual disability as a major feature --> obsolete X-linked congenital disorder of glycosylation with intellectual disability as a major feature
MONDO:0018286 non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature --> obsolete non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature
MONDO:0018287 congenital disorder of glycosylation with epilepsy as a major feature --> obsolete congenital disorder of glycosylation with epilepsy as a major feature
MONDO:0018290 congenital disorder of glycosylation with cardiac malformation as a major feature --> obsolete congenital disorder of glycosylation with cardiac malformation as a major feature
MONDO:0018294 congenital disorder of glycosylation with nephropathy as a major feature --> obsolete congenital disorder of glycosylation with nephropathy as a major feature
MONDO:0018295 congenital disorder of glycosylation with deafness as a major feature --> obsolete congenital disorder of glycosylation with deafness as a major feature
MONDO:0018377 rare hereditary disease with avascular necrosis --> obsolete rare hereditary disease with avascular necrosis
MONDO:0018386 rare male infertility due to hypothalamic-pituitary-gonadal axis disorder --> obsolete rare male infertility due to hypothalamic-pituitary-gonadal axis disorder
MONDO:0018387 rare male infertility due to adrenal disorder --> obsolete rare male infertility due to adrenal disorder
MONDO:0018388 rare male infertility due to testicular endocrine disorder --> obsolete rare male infertility due to testicular endocrine disorder
MONDO:0018396 rare male fertility disorder with obstructive azoospermia --> obsolete rare male fertility disorder with obstructive azoospermia
MONDO:0018397 female infertility due to hypothalamic-pituitary-gonadal axis disorder --> obsolete female infertility due to hypothalamic-pituitary-gonadal axis disorder
MONDO:0018400 rare female infertility due to an adrenal disorder --> obsolete rare female infertility due to an adrenal disorder
MONDO:0018401 female infertility due to an anomaly of ovarian function --> obsolete female infertility due to an anomaly of ovarian function
MONDO:0018405 rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin --> obsolete rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
MONDO:0018406 rare male infertility due to adrenal disorder of genetic origin --> obsolete rare male infertility due to adrenal disorder of genetic origin
MONDO:0018409 rare genetic disorder with obstructive azoospermia --> obsolete rare genetic disorder with obstructive azoospermia
MONDO:0018411 rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin --> obsolete rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
MONDO:0018412 rare female infertility due to adrenal disorder of genetic origin --> obsolete rare female infertility due to adrenal disorder of genetic origin
MONDO:0018413 female infertility due to an anomaly of ovarian function of genetic origin --> obsolete female infertility due to an anomaly of ovarian function of genetic origin
MONDO:0018455 dysostosis of genetic origin with limb anomaly as a major feature --> obsolete dysostosis of genetic origin with limb anomaly as a major feature
MONDO:0018457 rare genetic bone development disorder --> obsolete rare genetic bone development disorder
MONDO:0018488 rare genetic odontal or periodontal disorder --> obsolete rare genetic odontal or periodontal disorder
MONDO:0018520 rare epithelial tumor of pancreas --> obsolete rare epithelial tumor of pancreas
MONDO:0018530 rare epithelial tumor of liver and intrahepatic biliary tract --> obsolete rare epithelial tumor of liver and intrahepatic biliary tract
MONDO:0018539 rare epithelial tumor of small intestine --> obsolete rare epithelial tumor of small intestine
MONDO:0018719 obsolete rare capillary malformation with associated anomalies --> obsolete obsolete rare capillary malformation with associated anomalies
MONDO:0018721 rare combined vascular malformation --> obsolete rare combined vascular malformation
MONDO:0018723 rare vascular malformation of major vessels --> obsolete rare vascular malformation of major vessels
MONDO:0018730 rare genetic venous malformation --> obsolete rare genetic venous malformation
MONDO:0018753 rare disease with malignant hyperthermia --> obsolete rare disease with malignant hyperthermia
MONDO:0018798 other genetic dermis disorder --> obsolete other genetic dermis disorder
MONDO:0018833 rare idiopathic macular telangiectasia --> obsolete rare idiopathic macular telangiectasia
MONDO:0018880 rare teratologic disease --> obsolete rare teratologic disease
MONDO:0018972 rare epithelial tumor of stomach --> obsolete rare epithelial tumor of stomach
MONDO:0019014 mutilating palmoplantar keratoderma with periorificial keratotic plaques --> obsolete mutilating palmoplantar keratoderma with periorificial keratotic plaques
MONDO:0019038 rare maxillo-facial surgical disease --> obsolete rare maxillo-facial surgical disease
MONDO:0019039 rare hemorrhagic disorder due to a constitutional coagulation factors defect --> obsolete rare hemorrhagic disorder due to a constitutional coagulation factors defect
MONDO:0019061 rare parathyroid disease and phosphocalcic metabolism anomaly --> obsolete rare parathyroid disease and phosphocalcic metabolism anomaly
MONDO:0019097 hemorrhagic disorder due to a constitutional platelet anomaly --> obsolete hemorrhagic disorder due to a constitutional platelet anomaly
MONDO:0019252 other metabolic disease with skin involvement --> obsolete other metabolic disease with skin involvement
MONDO:0019274 other epidermal disorder --> obsolete other epidermal disorder
MONDO:0019275 other genetic epidermal disease --> obsolete other genetic epidermal disease
MONDO:0019304 rare photodermatosis --> obsolete rare photodermatosis
MONDO:0019546 other acquired skin disease --> obsolete other acquired skin disease
MONDO:0019590 rare endocrine growth disease --> obsolete rare endocrine growth disease
MONDO:0019602 other inborn metabolic disease --> obsolete other inborn metabolic disease
MONDO:0019663 short rib-polydactyly syndrome, Saldino-Noonan type --> obsolete short rib-polydactyly syndrome, Saldino-Noonan type
MONDO:0019744 rare renal tubular disease --> obsolete rare renal tubular disease
MONDO:0019748 rare cause of hypertension --> obsolete rare cause of hypertension
MONDO:0019936 rare otorhinolaryngological malformation --> obsolete rare otorhinolaryngological malformation
MONDO:0019937 rare gynecologic or obstetric disease --> obsolete rare gynecologic or obstetric disease
MONDO:0020013 rare odontologic disease --> obsolete rare odontologic disease
MONDO:0020014 rare disease with odontological manifestation --> obsolete rare disease with odontological manifestation
MONDO:0020016 rare neurologic disease with psychiatric involvement --> obsolete rare neurologic disease with psychiatric involvement
MONDO:0020035 rare otorhinolaryngologic tumor --> obsolete rare otorhinolaryngologic tumor
MONDO:0020094 autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature --> obsolete autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0020095 autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature --> obsolete autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature
MONDO:0020097 autosomal recessive disease with focal palmoplantar keratoderma as a major feature --> obsolete autosomal recessive disease with focal palmoplantar keratoderma as a major feature
MONDO:0020104 rare constitutional hemolytic anemia due to an enzyme disorder --> obsolete rare constitutional hemolytic anemia due to an enzyme disorder
MONDO:0020149 rare eye disease due to a differentiation anomaly --> obsolete rare eye disease due to a differentiation anomaly
MONDO:0020150 obsolete rare palpebral, lacrimal system and conjunctival disease --> obsolete obsolete rare palpebral, lacrimal system and conjunctival disease
MONDO:0020152 rare eyelid malformation --> obsolete rare eyelid malformation
MONDO:0020169 rare disorder with ptosis --> obsolete rare disorder with ptosis
MONDO:0020206 rare refraction anomaly --> obsolete rare refraction anomaly
MONDO:0020209 rare hyperopia and astigmatism --> obsolete rare hyperopia and astigmatism
MONDO:0020222 rare disease with glaucoma as a major feature --> obsolete rare disease with glaucoma as a major feature
MONDO:0020223 lens and zonula anomaly --> obsolete lens and zonula anomaly
MONDO:0020251 rare strabismus and restriction syndrome --> obsolete rare strabismus and restriction syndrome
MONDO:0020258 oculomotor apraxia or related oculomotor disease --> obsolete oculomotor apraxia or related oculomotor disease
MONDO:0020484 rare familial disorder with hypertrophic cardiomyopathy --> obsolete rare familial disorder with hypertrophic cardiomyopathy
MONDO:0020671 susceptibility to ischemic stroke --> obsolete susceptibility to ischemic stroke
MONDO:0020755 heart block --> obsolete heart block
MONDO:0020803 bundle branch block --> obsolete bundle branch block
MONDO:0021570 Hauptmann-Thannhauser muscular dystrophy --> obsolete Hauptmann-Thannhauser muscular dystrophy
MONDO:0022676 cataract - glaucoma --> obsolete cataract - glaucoma
MONDO:0022732 chorea minor --> obsolete chorea minor
MONDO:0025517 shrimp allergy --> obsolete shrimp allergy
MONDO:0025518 aspirin allergy --> obsolete aspirin allergy
MONDO:0028737 biliary atresia disorder --> obsolete biliary atresia disorder
MONDO:0044636 rare hyperkinetic movement disorder --> obsolete rare hyperkinetic movement disorder
MONDO:0044680 short rib-polydactyly syndrome type 5 --> obsolete short rib-polydactyly syndrome type 5
MONDO:0044808 early onset primary dystonia --> obsolete early onset primary dystonia
MONDO:0060649 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies --> obsolete short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies

Renaming

MONDO:0000606 gluten allergy --> obsolete gluten allergy
MONDO:0000772 pollen allergy --> obsolete pollen allergy
MONDO:0000773 Timothy grass allergy --> obsolete Timothy grass allergy
MONDO:0000776 metal allergy --> obsolete metal allergy
MONDO:0000779 apple allergy --> obsolete apple allergy
MONDO:0000780 apricot allergy --> obsolete apricot allergy
MONDO:0000783 orange allery --> orange allergy
MONDO:0000785 peach allergy --> obsolete peach allergy
MONDO:0000786 plum allergy --> obsolete plum allergy
MONDO:0000787 tomato allergy --> obsolete tomato allergy
MONDO:0000788 fish allergy --> obsolete fish allergy
MONDO:0000789 Atlantic cod allergy --> obsolete Atlantic cod allergy
MONDO:0000790 Atlantic salmon allergy --> obsolete Atlantic salmon allergy
MONDO:0000791 carp allergy --> obsolete carp allergy
MONDO:0000793 rainbow trout allergy --> obsolete rainbow trout allergy
MONDO:0000794 beta-lactam allergy --> obsolete beta-lactam allergy
MONDO:0000795 penicillin allergy --> obsolete penicillin allergy
MONDO:0000796 cow milk allergy (disease) --> obsolete cow milk allergy (disease)
MONDO:0000797 goat milk allergy --> obsolete goat milk allergy
MONDO:0000798 mollusc allergy --> obsolete mollusc allergy
MONDO:0000799 crustacean allergy --> obsolete crustacean allergy
MONDO:0000800 brown shrimp allergy --> obsolete brown shrimp allergy
MONDO:0000801 green mud crab allergy --> obsolete green mud crab allergy
MONDO:0000802 Indian prawn allergy --> obsolete Indian prawn allergy
MONDO:0000803 tiger prawn allergy --> obsolete tiger prawn allergy
MONDO:0000804 white shrimp allergy --> obsolete white shrimp allergy
MONDO:0000805 snail allergy --> obsolete snail allergy
MONDO:0000806 horned turban snail allergy --> obsolete horned turban snail allergy
MONDO:0000865 congenital fiber-type disproportion --> obsolete congenital fiber-type disproportion
MONDO:0000991 left bundle branch block --> obsolete left bundle branch block
MONDO:0001662 right bundle branch block (disease) --> obsolete right bundle branch block (disease)
MONDO:0002497 food allergy --> obsolete food allergy
MONDO:0002520 acute hepatic porphyria --> hepatic porphyria
MONDO:0005741 egg allergy --> obsolete egg allergy
MONDO:0006772 glycogen storage disease VIII --> obsolete glycogen storage disease VIII
MONDO:0006872 nut allergic reaction --> obsolete nut allergic reaction
MONDO:0007021 wheat allergic disease --> obsolete wheat allergic disease
MONDO:0007161 SPGF2 --> spermatogenic failure 2
MONDO:0007169 ATHS --> atherosclerosis susceptibility
MONDO:0007184 AGA1 --> alopecia, androgenetic, 1
MONDO:0007192 AABT --> beta-amino acids, renal transport of
MONDO:0007257 CANDF1 --> candidiasis, familial, 1
MONDO:0007332 SHFLD1 --> split-hand/foot malformation with long bone deficiency 1
MONDO:0007367 FEB1 --> febrile seizures, familial, 1
MONDO:0007559 PPR1 --> photoparoxysmal response 1
MONDO:0007729 DDH1 --> developmental dysplasia of the hip 1
MONDO:0007754 HYPRPP --> hyperhidrosis palmaris ET plantaris
MONDO:0007877 LAP --> laryngeal adductor paralysis
MONDO:0007918 microcephaly with or without chorioretinopathy, lymphedema, or mental retardation --> microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
MONDO:0007954 May-Hegglin anomaly --> obsolete May-Hegglin anomaly
MONDO:0007981 metachromatic leukodystrophy, adult-onset, with normal arylsulfatase a --> metachromatic leukodystrophy, adult-onset, with normal arylsulfatase A
MONDO:0007995 MCOPCT1 --> microphthalmia, isolated, with cataract 1
MONDO:0008032 autosomal dominant limb-girdle muscular dystrophy type 1A --> obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
MONDO:0008053 MYP2 --> myopia 2, autosomal dominant
MONDO:0008072 IGAN1 --> IgA nephropathy, susceptibility to, 1
MONDO:0008106 NYS2 --> nystagmus 2, congenital, autosomal dominant
MONDO:0008164 OTSC1 --> otosclerosis 1
MONDO:0008172 PHOAD --> hypertrophic osteoarthropathy, primary, autosomal dominant
MONDO:0008290 POROK1 --> porokeratosis 1, Mibelli type
MONDO:0008414 SCZD1 --> schizophrenia 1
MONDO:0008614 ST3 --> suppressor of tumorigenicity 3
MONDO:0008646 long QT syndrome 1 --> obsolete long QT syndrome 1
MONDO:0008653 VUR1 --> vesicoureteral reflux 1
MONDO:0008654 NYS4 --> nystagmus 4, congenital, autosomal dominant
MONDO:0008776 amyloidosis of gingiva and conjunctiva, with mental retardation --> amyloidosis of gingiva and conjunctiva, with intellectual disability
MONDO:0008820 arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies --> arthrogryposis, distal, with hypopituitarism, intellectual disability, and facial anomalies
MONDO:0008821 arthrogryposis, distal, with mental retardation and characteristic facies --> arthrogryposis, distal, with intellectual disability and characteristic facies
MONDO:0008932 PCD --> premature centromere division
MONDO:0008942 CPD2 --> cerebelloparenchymal disorder II
MONDO:0009040 craniosynostosis-mental retardation syndrome of 51N and Gettig --> craniosynostosis-intellectual disability syndrome of 51N and Gettig
MONDO:0009041 craniosynostosis-mental retardation-clefting syndrome --> craniosynostosis-intellectual disability-clefting syndrome
MONDO:0009056 cutis verticis gyrata and mental retardation --> cutis verticis gyrata and intellectual disability
MONDO:0009128 dwarfism, mental retardation, and eye abnormality --> dwarfism, intellectual disability, and eye abnormality
MONDO:0009186 epilepsy, photogenic, with spastic diplegia and mental retardation --> epilepsy, photogenic, with spastic diplegia and intellectual disability
MONDO:0009201 facial abnormalities, kyphoscoliosis, and mental retardation --> facial abnormalities, kyphoscoliosis, and intellectual disability
MONDO:0009317 nonphotosensitive trichothiodystrophy --> obsolete nonphotosensitive trichothiodystrophy
MONDO:0009382 PSHB --> hyperbilirubinemia, shunt, primary
MONDO:0009460 Indolylacroyl Glycinuria with mental retardation --> indolylacroyl glycinuria with intellectual disability
MONDO:0009641 mitochondrial complex II deficiency --> obsolete mitochondrial complex II deficiency
MONDO:0009649 MYMY1 --> moyamoya disease 1
MONDO:0009713 MYP18 --> myopia 18, autosomal recessive
MONDO:0009739 infantile neuroaxonal dystrophy --> obsolete infantile neuroaxonal dystrophy
MONDO:0009913 prune belly syndrome with pulmonic stenosis, mental retardation, and deafness --> prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness
MONDO:0009986 retinopathy, pigmentary, and mental retardation --> retinopathy, pigmentary, and intellectual disability
MONDO:0010040 ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation --> ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability
MONDO:0010042 spastic diplegia and mental retardation --> spastic diplegia and intellectual disability
MONDO:0010054 spinal muscular atrophy with mental retardation --> spinal muscular atrophy with intellectual disability
MONDO:0010070 BCYM1A --> brachyolmia type 1, Hobaek type
MONDO:0010074 BCYM1B --> brachyolmia type 1, toledo type
MONDO:0010084 sucrosuria, hiatus hernia and mental retardation --> sucrosuria, hiatus hernia and intellectual disability
MONDO:0010086 sudden infant death syndrome --> obsolete sudden infant death syndrome
MONDO:0010189 vitiligo, progressive, with mental retardation and urethral duplication --> vitiligo, progressive, with intellectual disability and urethral duplication
MONDO:0010228 DFNX3 --> deafness, X-linked 3
MONDO:0010230 MRX23 --> intellectual disability, X-linked 23
MONDO:0010231 MRX20 --> intellectual disability, X-linked 20
MONDO:0010236 MRX14 --> intellectual disability, X-linked 14
MONDO:0010250 MRX49 --> intellectual disability, X-linked 49
MONDO:0010251 MRX50 --> intellectual disability, X-linked 50
MONDO:0010257 HPCX1 --> prostate cancer, hereditary, X-linked 1
MONDO:0010260 ACLLX --> arthrogryposis, congenital, lower limb, X-linked
MONDO:0010267 EMWX --> episodic muscle weakness, X-linked
MONDO:0010274 TGCT1 --> testicular germ cell tumor 1
MONDO:0010300 MRX53 --> intellectual disability, X-linked 53
MONDO:0010301 THCYTX --> thrombocythemia, X-linked
MONDO:0010307 MRX73 --> intellectual disability, X-linked 73
MONDO:0010309 MRX42 --> intellectual disability, X-linked 42
MONDO:0010314 BPPX --> polymicrogyria, bilateral perisylvian, X-linked
MONDO:0010322 MRX2 --> intellectual disability, X-linked 2
MONDO:0010324 MRX81 --> intellectual disability, X-linked 81
MONDO:0010329 MRX77 --> intellectual disability, X-linked 77
MONDO:0010347 MRX84 --> intellectual disability, X-linked 84
MONDO:0010351 Fanconi anemia complementation group b --> Fanconi anemia complementation group B
MONDO:0010352 MRX82 --> intellectual disability, X-linked 82
MONDO:0010360 PARK12 --> parkinson disease 12
MONDO:0010365 CFTDX --> myopathy, congenital, with fiber-type disproportion, X-linked
MONDO:0010369 NYS5 --> nystagmus 5, congenital, X-linked
MONDO:0010377 MYP13 --> myopia 13, X-linked
MONDO:0010380 cataract, ataxia, short stature, and mental retardation --> cataract, ataxia, short stature, and intellectual disability
MONDO:0010388 rolandic epilepsy, mental retardation, and speech dyspraxia, X-linked --> rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
MONDO:0010405 HPCX2 --> prostate cancer, hereditary, X-linked 2
MONDO:0010410 AGA2 --> alopecia, androgenetic, 2
MONDO:0010413 MRX95 --> intellectual disability, X-linked 95
MONDO:0010450 MRX89 --> intellectual disability, X-linked 89
MONDO:0010453 MRX92 --> intellectual disability, X-linked 92
MONDO:0010454 MRX88 --> intellectual disability, XMEN-linked 88
MONDO:0010468 ANIB5 --> aneurysm, intracranial berry, 5
MONDO:0010486 palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked --> Olmsted syndrome, X-linked
MONDO:0010573 cutis verticis gyrata, thyroid aplasia, and mental retardation --> cutis verticis gyrata, thyroid aplasia, and intellectual disability
MONDO:0010685 MYP1 --> myopia 1, X-linked
MONDO:0010697 OPEM --> ophthalmoplegia, external, and myopia
MONDO:0010834 HSCR5 --> hirschsprung disease, susceptibility to, 5
MONDO:0010836 NNO1 --> nanophthalmos 1
MONDO:0010846 EXT3 --> exostoses, multiple, type III
MONDO:0010872 PDDP --> parotid salivary glands, polycystic dysgenetic disease of
MONDO:0010897 SCZD3 --> schizophrenia 3
MONDO:0010910 ENUR1 --> enuresis, nocturnal, 1
MONDO:0010957 agonadism, 46,XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations --> agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformations
MONDO:0010968 GLC3B --> glaucoma 3, primary infantile, B
MONDO:0010982 ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin --> ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin
MONDO:0010985 FAME1 --> epilepsy, familial adult myoclonic, 1
MONDO:0011021 neuronal intestinal dysplasia, type b --> neuronal intestinal dysplasia, type B
MONDO:0011072 NIDDM2 --> diabetes mellitus, noninsulin-dependent, 2
MONDO:0011084 PSORS3 --> psoriasis 3, susceptibility to
MONDO:0011175 FRDA2 --> friedreich ataxia 2
MONDO:0011201 ETM2 --> tremor, hereditary essential, 2
MONDO:0011220 PARK3 --> parkinson disease 3, autosomal dominant
MONDO:0011222 GLC1D --> glaucoma 1, open angle, D
MONDO:0011231 FEB2 --> febrile seizures, familial, 2
MONDO:0011250 microcephaly, macrotia, and mental retardation --> microcephaly, macrotia, and intellectual disability
MONDO:0011256 emphysema, congenital, with deafness, penoscrotal web, and mental retardation --> emphysema, congenital, with deafness, penoscrotal web, and intellectual disability
MONDO:0011261 spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation --> spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability
MONDO:0011265 STHAG2 --> tooth agenesis, selective, 2
MONDO:0011280 SCZD6 --> schizophrenia 6
MONDO:0011290 dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation --> dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability
MONDO:0011294 SCZD5 --> schizophrenia 5
MONDO:0011295 SCZD7 --> schizophrenia 7
MONDO:0011298 SCZD8 --> schizophrenia 8
MONDO:0011300 MYP3 --> myopia 3, autosomal dominant
MONDO:0011307 SCZD2 --> schizophrenia 2
MONDO:0011311 glaucoma 1, open angle, f --> glaucoma 1, open angle, F
MONDO:0011325 Fanconi anemia complementation group f --> Fanconi anemia complementation group F
MONDO:0011341 microcephaly, facial abnormalities, micromelia, and mental retardation --> microcephaly, facial abnormalities, micromelia, and intellectual disability
MONDO:0011387 PSORS4 --> psoriasis 4, susceptibility to
MONDO:0011433 anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome --> anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome
MONDO:0011434 PSORS5 --> psoriasis 5, susceptibility to
MONDO:0011478 growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia --> growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia
MONDO:0011491 EIG7 --> epilepsy, idiopathic generalized, susceptibility to, 7
MONDO:0011542 PSORS6 --> psoriasis 6, susceptibility to
MONDO:0011550 fibromatosis, gingival, with hypertrichosis and mental retardation --> fibromatosis, gingival, with hypertrichosis and intellectual disability
MONDO:0011552 SCZD10 --> schizophrenia 10
MONDO:0011554 DFNM1 --> deafness, nonsyndromic, modifier 1
MONDO:0011556 BCC1 --> basal cell carcinoma, susceptibility to, 1
MONDO:0011563 GINGF2 --> fibromatosis, gingival, 2
MONDO:0011573 PSORS7 --> psoriasis 7, susceptibility to
MONDO:0011586 OTSC2 --> otosclerosis 2
MONDO:0011592 EVR3 --> exudative vitreoretinopathy 3
MONDO:0011611 short stature, mental retardation, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting --> short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting
MONDO:0011627 AUTS5 --> autism, susceptibility to, 5
MONDO:0011656 PDB4 --> paget disease of bone 4
MONDO:0011659 HTX3 --> heterotaxy, visceral, 3, autosomal
MONDO:0011674 Charcot-Marie-Tooth disease dominant intermediate b --> Charcot-Marie-Tooth disease dominant intermediate B
MONDO:0011675 Charcot-Marie-Tooth disease dominant intermediate a --> Charcot-Marie-Tooth disease dominant intermediate A
MONDO:0011692 IBGC2 --> basal ganglia calcification, idiopathic, 2
MONDO:0011704 GLC1B --> glaucoma 1, open angle, B
MONDO:0011733 PSMNSB --> parasomnia, sleep bruxism type
MONDO:0011736 Cree mental retardation syndrome --> Cree intellectual disability syndrome
MONDO:0011737 PARK10 --> parkinson disease 10
MONDO:0011741 HSCR6 --> hirschsprung disease, susceptibility to, 6
MONDO:0011742 HSCR7 --> hirschsprung disease, susceptibility to, 7
MONDO:0011753 EIG2 --> epilepsy, idiopathic generalized, susceptibility to, 2
MONDO:0011755 SLSN3 --> senior-loken syndrome 3
MONDO:0011793 CELIAC5 --> celiac disease, susceptibility to, 5
MONDO:0011796 PEPS --> epilepsy, partial, with pericentral spikes
MONDO:0011800 GLM4 --> glioma susceptibility 4
MONDO:0011824 AUTS8 --> autism, susceptibility to, 8
MONDO:0011858 spastic paraplegia, ataxia, and mental retardation --> spastic paraplegia, ataxia, and intellectual disability
MONDO:0011860 LPRS2 --> leprosy, susceptibility to, 2
MONDO:0011880 CANDF3 --> candidiasis, familial, 3
MONDO:0011900 POROK4 --> porokeratosis 4, disseminated superficial actinic type
MONDO:0011909 Charcot-Marie-Tooth disease dominant intermediate d --> Charcot-Marie-Tooth disease dominant intermediate D
MONDO:0011915 MMVP2 --> mitral valve prolapse, myxomatous 2
MONDO:0011926 PSORS9 --> psoriasis 9, susceptibility to
MONDO:0011931 OVCAS1 --> ovarian cancer, susceptibility to, 1
MONDO:0011954 CMM4 --> melanoma, cutaneous malignant, susceptibility to, 4
MONDO:0011956 AUTS3 --> autism, susceptibility to, 3
MONDO:0011990 BFNS3 --> seizures, benign familial neonatal, 3
MONDO:0011999 OTSC3 --> otosclerosis 3
MONDO:0012005 growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy --> growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy
MONDO:0012012 Charcot-Marie-Tooth disease dominant intermediate c --> Charcot-Marie-Tooth disease dominant intermediate C
MONDO:0012014 Charcot-Marie-Tooth disease recessive intermediate a --> Charcot-Marie-Tooth disease recessive intermediate A
MONDO:0012015 NYS3 --> nystagmus 3, congenital, autosomal dominant
MONDO:0012021 MYP17 --> myopia 17, autosomal dominant
MONDO:0012027 AIS2 --> autoimmune disease, susceptibility to, 2
MONDO:0012028 AIS3 --> autoimmune disease, susceptibility to, 3
MONDO:0012042 HSCR8 --> hirschsprung disease, susceptibility to, 8
MONDO:0012045 MYP5 --> myopia 5, autosomal dominant
MONDO:0012053 ANIB2 --> aneurysm, intracranial berry, 2
MONDO:0012066 ATFB1 --> atrial fibrillation, familial, 1
MONDO:0012069 KTCN3 --> keratoconus 3
MONDO:0012079 ASPG2 --> asperger syndrome, susceptibility to, 2
MONDO:0012082 ASPG1 --> asperger syndrome, susceptibility to, 1
MONDO:0012101 GLC1J --> glaucoma 1, open angle, J
MONDO:0012102 GLC1K --> glaucoma 1, open angle, K
MONDO:0012113 EIG3 --> epilepsy, idiopathic generalized, susceptibility to, 3
MONDO:0012119 ASPG3 --> asperger syndrome, susceptibility to, 3
MONDO:0012121 OTSC5 --> otosclerosis 5
MONDO:0012122 MYMY3 --> moyamoya disease 3
MONDO:0012134 EJM3 --> myoclonic epilepsy, juvenile, susceptibility to, 3
MONDO:0012158 KTCN2 --> keratoconus 2
MONDO:0012159 LNCR1 --> lung cancer susceptibility 1
MONDO:0012167 ATFB2 --> atrial fibrillation, familial, 2
MONDO:0012187 Fanconi anemia complementation group j --> Fanconi anemia complementation group J
MONDO:0012194 ANIB3 --> aneurysm, intracranial berry, 3
MONDO:0012214 GCCD3 --> glucocorticoid deficiency 3
MONDO:0012218 ADDWOC --> dandy-walker malformation with occipital cephalocele, autosomal dominant
MONDO:0012224 FEB6 --> febrile seizures, familial, 6
MONDO:0012226 FEB5 --> febrile seizures, familial, 5
MONDO:0012227 MYP7 --> myopia 7
MONDO:0012228 MYP8 --> myopia 8
MONDO:0012229 MYP9 --> myopia 9
MONDO:0012230 MYP10 --> myopia 10
MONDO:0012236 KTCN4 --> keratoconus 4
MONDO:0012242 VVS --> syncope, familial vasovagal
MONDO:0012261 AUTS6 --> autism, susceptibility to, 6
MONDO:0012262 CFEOM3C --> fibrosis of extraocular muscles, congenital, 3c
MONDO:0012263 AIS4 --> autoimmune disease, susceptibility to, 4
MONDO:0012264 PEE2 --> preeclampsia/eclampsia 2
MONDO:0012265 PEE3 --> preeclampsia/eclampsia 3
MONDO:0012285 LVNC2 --> left ventricular noncompaction 2
MONDO:0012302 PFM3 --> parietal foramina 3
MONDO:0012304 PPR2 --> photoparoxysmal response 2
MONDO:0012305 PPR3 --> photoparoxysmal response 3
MONDO:0012324 14q22q23 microdeletion syndrome --> Frias syndrome
MONDO:0012337 GLC1I --> glaucoma 1, open angle, I
MONDO:0012338 EIG4 --> epilepsy, idiopathic generalized, susceptibility to, 4
MONDO:0012340 CELIAC2 --> celiac disease, susceptibility to, 2
MONDO:0012343 AAA2 --> aortic aneurysm, familial abdominal, 2
MONDO:0012346 GEFSP4 --> generalized epilepsy with febrile seizures plus, type 4
MONDO:0012358 LPRS1 --> leprosy, susceptibility to, 1
MONDO:0012365 GBD2 --> gallbladder disease 2
MONDO:0012366 GBD3 --> gallbladder disease 3
MONDO:0012377 ASPG4 --> asperger syndrome, susceptibility to, 4
MONDO:0012378 GINGF3 --> fibromatosis, gingival, 3
MONDO:0012388 MYP11 --> myopia 11, autosomal dominant
MONDO:0012389 MYP12 --> myopia 12, autosomal dominant
MONDO:0012425 FECD2 --> corneal dystrophy, fuchs endothelial, 2
MONDO:0012428 KYPSC1 --> kyphoscoliosis 1
MONDO:0012430 cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 --> cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2
MONDO:0012443 ANIB4 --> aneurysm, intracranial berry, 4
MONDO:0012451 EOE1 --> esophagitis, eosinophilic, 1
MONDO:0012469 MYP14 --> myopia 14
MONDO:0012470 HPC7 --> prostate cancer, hereditary, 7
MONDO:0012515 GLC1M --> glaucoma 1, open angle, M
MONDO:0012533 AUTS7 --> autism, susceptibility to, 7
MONDO:0012537 SHFLD2 --> split-hand/foot malformation with long bone deficiency 2
MONDO:0012542 PSORS8 --> psoriasis 8, susceptibility to
MONDO:0012566 AUTS11 --> autism, susceptibility to, 11
MONDO:0012567 AUTS12 --> autism, susceptibility to, 12
MONDO:0012568 OS4 --> osteoarthritis susceptibility 4
MONDO:0012569 MMVP3 --> mitral valve prolapse, myxomatous 3
MONDO:0012578 AUTS13 --> autism, susceptibility to, 13
MONDO:0012583 STHAG5 --> tooth agenesis, selective, 5
MONDO:0012598 GINGF4 --> fibromatosis, gingival, 4
MONDO:0012599 HYT8 --> hypertension, essential, susceptibility to, 8
MONDO:0012600 AUTS9 --> autism, susceptibility to, 9
MONDO:0012601 AUTS10 --> autism, susceptibility to, 10
MONDO:0012617 MRT9 --> intellectual disability, autosomal recessive 9
MONDO:0012618 MRT10 --> intellectual disability, autosomal recessive 10
MONDO:0012619 MRT11 --> intellectual disability, autosomal recessive 11
MONDO:0012620 HPC10 --> prostate cancer, hereditary, 10
MONDO:0012623 MRT4 --> intellectual disability, autosomal recessive 4
MONDO:0012628 CHDS8 --> coronary heart disease, susceptibility to, 8
MONDO:0012632 Alzheimer disease 15 --> obsolete Alzheimer disease 15
MONDO:0012645 GLC1N --> glaucoma 1, open angle, N
MONDO:0012646 GLC1H --> glaucoma 1, open angle, H
MONDO:0012653 PHPVAD --> persistent hyperplastic primary vitreous, autosomal dominant
MONDO:0012655 EJM4 --> myoclonic epilepsy, juvenile, susceptibility to, 4
MONDO:0012671 ETM3 --> tremor, hereditary essential, 3
MONDO:0012673 CRCS2 --> colorectal cancer, susceptibility to, 2
MONDO:0012678 ATFB5 --> atrial fibrillation, familial, 5
MONDO:0012681 FEB7 --> febrile seizures, familial, 7
MONDO:0012692 renal tubular acidosis, distal, with nephrocalcinosis, short stature, mental retardation, and distinctive facies --> renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies
MONDO:0012696 OTSC4 --> otosclerosis 4
MONDO:0012697 OTSC7 --> otosclerosis 7
MONDO:0012702 CELIAC6 --> celiac disease, susceptibility to, 6
MONDO:0012708 PLSA1 --> primary lateral sclerosis, adult, 1
MONDO:0012710 HSCR9 --> hirschsprung disease, susceptibility to, 9
MONDO:0012712 DYTCA --> dystonia with cerebellar atrophy
MONDO:0012751 AAA3 --> aortic aneurysm, familial abdominal, 3
MONDO:0012752 ANIB6 --> aneurysm, intracranial berry, 6
MONDO:0012754 NNO3 --> nanophthalmos 3
MONDO:0012760 EIG5 --> epilepsy, idiopathic generalized, susceptibility to, 5
MONDO:0012768 HPC11 --> prostate cancer, hereditary, 11
MONDO:0012769 HPC14 --> prostate cancer, hereditary, 14
MONDO:0012770 HPC15 --> prostate cancer, hereditary, 15
MONDO:0012776 CELIAC7 --> celiac disease, susceptibility to, 7
MONDO:0012777 CELIAC8 --> celiac disease, susceptibility to, 8
MONDO:0012778 CELIAC9 --> celiac disease, susceptibility to, 9
MONDO:0012779 CELIAC10 --> celiac disease, susceptibility to, 10
MONDO:0012780 CELIAC11 --> celiac disease, susceptibility to, 11
MONDO:0012781 CELIAC12 --> celiac disease, susceptibility to, 12
MONDO:0012782 CELIAC13 --> celiac disease, susceptibility to, 13
MONDO:0012788 CHDS9 --> coronary heart disease, susceptibility to, 9
MONDO:0012797 OTSC8 --> otosclerosis 8
MONDO:0012810 ANIB7 --> aneurysm, intracranial berry, 7
MONDO:0012811 ANIB8 --> aneurysm, intracranial berry, 8
MONDO:0012821 CRCS5 --> colorectal cancer, susceptibility to, 5
MONDO:0012822 CRCS6 --> colorectal cancer, susceptibility to, 6
MONDO:0012823 CRCS7 --> colorectal cancer, susceptibility to, 7
MONDO:0012846 GEFSP6 --> generalized epilepsy with febrile seizures plus, type 6
MONDO:0012857 POROK5 --> porokeratosis 5, disseminated superficial actinic type
MONDO:0012872 THPH9 --> thrombophilia, familial, due to decreased release of tissue plasminogen activator
MONDO:0012874 POROK6 --> porokeratosis 6, disseminated superficial actinic type
MONDO:0012889 SS3 --> sarcoidosis, susceptibility to, 3
MONDO:0012894 OS6 --> osteoarthritis susceptibility 6
MONDO:0012896 PSORS10 --> psoriasis 10, susceptibility to
MONDO:0012899 AGA3 --> alopecia, androgenetic, 3
MONDO:0012909 skeletal defects, genital hypoplasia, and mental retardation --> skeletal defects, genital hypoplasia, and intellectual disability
MONDO:0012913 Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome --> Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome
MONDO:0012932 MYP16 --> myopia 16, autosomal dominant
MONDO:0012942 LNCR3 --> lung cancer susceptibility 3
MONDO:0012949 ANIB9 --> aneurysm, intracranial berry, 9
MONDO:0012950 ANIB10 --> aneurysm, intracranial berry, 10
MONDO:0012951 CRCS8 --> colorectal cancer, susceptibility to, 8
MONDO:0012952 CRCS9 --> colorectal cancer, susceptibility to, 9
MONDO:0012959 PSORS11 --> psoriasis 11, susceptibility to
MONDO:0012965 BFIS4 --> seizures, benign familial infantile, 4
MONDO:0012972 FEB10 --> febrile seizures, familial, 10
MONDO:0012995 MYP15 --> myopia 15, autosomal dominant
MONDO:0013055 Stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic features --> Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features
MONDO:0013057 PSORS12 --> psoriasis 12, susceptibility to
MONDO:0013084 NBLST4 --> neuroblastoma, susceptibility to, 4
MONDO:0013085 NBLST5 --> neuroblastoma, susceptibility to, 5
MONDO:0013086 NBLST6 --> neuroblastoma, susceptibility to, 6
MONDO:0013088 FL1 --> follicular lymphoma, susceptibility to, 1
MONDO:0013089 SCZD13 --> schizophrenia 13
MONDO:0013094 GLM5 --> glioma susceptibility 5
MONDO:0013095 GLM6 --> glioma susceptibility 6
MONDO:0013096 GLM7 --> glioma susceptibility 7
MONDO:0013097 GLM8 --> glioma susceptibility 8
MONDO:0013100 ATFB8 --> atrial fibrillation, familial, 8
MONDO:0013101 BCC2 --> basal cell carcinoma, susceptibility to, 2
MONDO:0013102 BCC3 --> basal cell carcinoma, susceptibility to, 3
MONDO:0013104 BCC4 --> basal cell carcinoma, susceptibility to, 4
MONDO:0013105 BCC5 --> basal cell carcinoma, susceptibility to, 5
MONDO:0013106 BCC6 --> basal cell carcinoma, susceptibility to, 6
MONDO:0013121 GLC3C --> glaucoma 3, primary congenital, C
MONDO:0013122 glaucoma 3, primary congenital, d --> glaucoma 3, primary congenital, D
MONDO:0013151 CACD3 --> choroidal dystrophy, central areolar, 3
MONDO:0013155 muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B3 --> muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
MONDO:0013156 muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B4 --> muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
MONDO:0013159 muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B1 --> muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
MONDO:0013160 muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 --> muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
MONDO:0013167 PARK16 --> parkinson disease 16
MONDO:0013188 cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 --> cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3
MONDO:0013205 FECD5 --> corneal dystrophy, fuchs endothelial, 5
MONDO:0013207 FECD7 --> corneal dystrophy, fuchs endothelial, 7
MONDO:0013213 CIHL --> hearing loss, cisplatin-induced, susceptibility to
MONDO:0013246 NAFLD2 --> fatty liver disease, nonalcoholic, susceptibility to, 2
MONDO:0013257 LPRS6 --> leprosy, susceptibility to, 6
MONDO:0013260 EOE2 --> esophagitis, eosinophilic, 2
MONDO:0013321 FWS --> forsythe-wakeling syndrome
MONDO:0013322 FAME3 --> epilepsy, familial adult myoclonic, 3
MONDO:0013332 brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation --> brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability
MONDO:0013338 Charcot-Marie-Tooth disease recessive intermediate b --> Charcot-Marie-Tooth disease recessive intermediate B
MONDO:0013448 GEFSP8 --> generalized epilepsy with febrile seizures plus, type 8
MONDO:0013488 APLDC3 --> lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis
MONDO:0013491 megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation --> megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability
MONDO:0013492 APMR3 --> alopecia-intellectual disability syndrome 3
MONDO:0013493 ACACAD --> acetyl-coa carboxylase deficiency
MONDO:0013496 IGAN2 --> IgA nephropathy, susceptibility to, 2
MONDO:0013508 MYP19 --> myopia 19, autosomal dominant
MONDO:0013603 MYP20 --> myopia 20, autosomal dominant
MONDO:0013629 MRT16 --> intellectual disability, autosomal recessive 16
MONDO:0013631 LNCR5 --> lung cancer susceptibility 5
MONDO:0013654 ANIB11 --> aneurysm, intracranial berry, 11
MONDO:0013665 EJM9 --> epilepsy, juvenile myoclonic, susceptibility to, 9
MONDO:0013682 VUR4 --> vesicoureteral reflux 4
MONDO:0013683 VUR5 --> vesicoureteral reflux 5
MONDO:0013684 VUR6 --> vesicoureteral reflux 6
MONDO:0013694 MRT31 --> intellectual disability, autosomal recessive 31
MONDO:0013697 MRT29 --> intellectual disability, autosomal recessive 29
MONDO:0013703 MRT33 --> intellectual disability, autosomal recessive 33
MONDO:0013704 MRT30 --> intellectual disability, autosomal recessive 30
MONDO:0013705 MRT19 --> intellectual disability, autosomal recessive 19
MONDO:0013706 MRT23 --> intellectual disability, autosomal recessive 23
MONDO:0013707 MRT24 --> intellectual disability, autosomal recessive 24
MONDO:0013708 MRT25 --> intellectual disability, autosomal recessive 25
MONDO:0013709 MRT28 --> intellectual disability, autosomal recessive 28
MONDO:0013716 AAA4 --> aortic aneurysm, familial abdominal, 4
MONDO:0013814 PDCOS --> podoconiosis, susceptibility to
MONDO:0013830 KTCN5 --> keratoconus 5
MONDO:0013831 KTCN6 --> keratoconus 6
MONDO:0013832 KTCN8 --> keratoconus 8
MONDO:0013833 KTCN7 --> keratoconus 7
MONDO:0013856 hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes --> hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes
MONDO:0013868 POROK7 --> porokeratosis 7, disseminated superficial actinic type
MONDO:0013886 nonprogressive cerebellar atxia with mental retardation --> nonprogressive cerebellar atxia with intellectual disability
MONDO:0013903 NYS7 --> nystagmus 7, congenital, autosomal dominant
MONDO:0013908 TTPP3 --> thyrotoxic periodic paralysis, susceptibility to, 3
MONDO:0013909 HHV8S --> human herpesvirus 8, susceptibility to
MONDO:0013973 ECTD5 --> ectodermal dysplasia 5, hair/nail type
MONDO:0013974 ECTD6 --> ectodermal dysplasia 6, hair/nail type
MONDO:0013980 PPKP1B --> palmoplantar keratoderma, punctate type ib
MONDO:0013988 CHTD3 --> congenital heart defects, multiple types, 3
MONDO:0014055 FAME4 --> epilepsy, familial adult myoclonic, 4
MONDO:0014074 Charcot-Marie-Tooth disease dominant intermediate f --> Charcot-Marie-Tooth disease dominant intermediate F
MONDO:0014104 cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 --> cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4
MONDO:0014141 muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B14 --> muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
MONDO:0014154 Charcot-Marie-Tooth disease recessive intermediate c --> Charcot-Marie-Tooth disease recessive intermediate C
MONDO:0014161 VUR7 --> vesicoureteral reflux 7
MONDO:0014219 alacrima, achalasia, and mental retardation syndrome --> alacrima, achalasia, and intellectual disability syndrome
MONDO:0014264 OTSC10 --> otosclerosis 10
MONDO:0014277 DDH2 --> developmental dysplasia of the hip 2
MONDO:0014301 DDD3 --> dowling-degos disease 3
MONDO:0014467 Charcot-Marie-Tooth disease recessive intermediate d --> Charcot-Marie-Tooth disease recessive intermediate D
MONDO:0014986 Fanconi anemia complementation group r --> Fanconi anemia complementation group R
MONDO:0015147 other syndrome with lissencephaly as a major feature --> obsolete other syndrome with lissencephaly as a major feature
MONDO:0015226 syndrome with limb malformations as a major feature --> obsolete syndrome with limb malformations as a major feature
MONDO:0015319 rare disease with Pierre Robin syndrome --> obsolete rare disease with Pierre Robin syndrome
MONDO:0015332 rare developmental defect with connective tissue involvement --> obsolete rare developmental defect with connective tissue involvement
MONDO:0015475 rare head and neck malformation --> obsolete rare head and neck malformation
MONDO:0015506 rare syndrome with cardiac malformations --> obsolete rare syndrome with cardiac malformations
MONDO:0015603 rare odontal or periodontal disorder --> obsolete rare odontal or periodontal disorder
MONDO:0015652 chromosomal anomaly with epilepsy as a major feature --> obsolete chromosomal anomaly with epilepsy as a major feature
MONDO:0015662 hemorrhagic disorder due to an acquired coagulation factor defect --> obsolete hemorrhagic disorder due to an acquired coagulation factor defect
MONDO:0015669 rare disease with dentinogenesis imperfecta --> obsolete rare disease with dentinogenesis imperfecta
MONDO:0015847 rare vaginal malformation --> obsolete rare vaginal malformation
MONDO:0015851 rare breast malformation --> obsolete rare breast malformation
MONDO:0015857 rare non-malformative gynecologic or obstetric disease --> obsolete rare non-malformative gynecologic or obstetric disease
MONDO:0015858 rare non-malformative breast disease --> obsolete rare non-malformative breast disease
MONDO:0015859 rare non-malformative uterovaginal or vulvovaginal disease --> obsolete rare non-malformative uterovaginal or vulvovaginal disease
MONDO:0015861 rare uterine adnexal tumor --> obsolete rare uterine adnexal tumor
MONDO:0015875 rare non-malformative uterine adnexal disease --> obsolete rare non-malformative uterine adnexal disease
MONDO:0015876 rare vulvovaginal tumor --> obsolete rare vulvovaginal tumor
MONDO:0015885 rare insulin-resistance syndrome --> obsolete rare insulin-resistance syndrome
MONDO:0015887 rare diabetes mellitus type 2 --> obsolete rare diabetes mellitus type 2
MONDO:0015888 other rare diabetes mellitus --> obsolete other rare diabetes mellitus
MONDO:0015889 rare hypothalamic or pituitary disease --> obsolete rare hypothalamic or pituitary disease
MONDO:0015890 rare disorder with congenital hypogonadotropic hypogonadism --> obsolete rare disorder with congenital hypogonadotropic hypogonadism
MONDO:0015912 MYH-9 related disease --> macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
MONDO:0015913 rare thrombotic disease of hematologic origin --> obsolete rare thrombotic disease of hematologic origin
MONDO:0015916 rare neuroinflammatory or neuroimmunological disease --> obsolete rare neuroinflammatory or neuroimmunological disease
MONDO:0015937 rare inflammatory eye disease --> obsolete rare inflammatory eye disease
MONDO:0015964 obsolete rare genetic palpebral, lacrimal system and conjunctival disease --> obsolete obsolete rare genetic palpebral, lacrimal system and conjunctival disease
MONDO:0015965 rare genetic refraction anomaly --> obsolete rare genetic refraction anomaly
MONDO:0015968 rare genetic hypothalamic or pituitary disease --> obsolete rare genetic hypothalamic or pituitary disease
MONDO:0015970 rare genetic parathyroid disease and phosphocalcic metabolism disorder --> obsolete rare genetic parathyroid disease and phosphocalcic metabolism disorder
MONDO:0016055 syndrome with corpus callosum agenesis /dysgenesis as a major feature --> obsolete syndrome with corpus callosum agenesis /dysgenesis as a major feature
MONDO:0016132 rare hereditary disease with peripheral neuropathy --> obsolete rare hereditary disease with peripheral neuropathy
MONDO:0016133 rare hereditary metabolic disease with peripheral neuropathy --> obsolete rare hereditary metabolic disease with peripheral neuropathy
MONDO:0016134 rare hereditary systemic disease with peripheral neuropathy --> obsolete rare hereditary systemic disease with peripheral neuropathy
MONDO:0016135 rare hereditary neurologic disease with peripheral neuropathy --> obsolete rare hereditary neurologic disease with peripheral neuropathy
MONDO:0016232 rare venous malformation --> obsolete rare venous malformation
MONDO:0016233 rare lymphatic system malformation --> obsolete rare lymphatic system malformation
MONDO:0016320 rare hereditary thrombophilia --> obsolete rare hereditary thrombophilia
MONDO:0016406 other metabolic disease with epilepsy --> obsolete other metabolic disease with epilepsy
MONDO:0016507 rare surgically correctable form of primary aldosteronism --> obsolete rare surgically correctable form of primary aldosteronism
MONDO:0016508 rare non surgically correctable form of primary aldosteronism --> obsolete rare non surgically correctable form of primary aldosteronism
MONDO:0016631 hemorrhagic disorder due to an acquired platelet anomaly --> obsolete hemorrhagic disorder due to an acquired platelet anomaly
MONDO:0016633 thrombotic disorder due to a constitutional coagulation factors defect --> obsolete thrombotic disorder due to a constitutional coagulation factors defect
MONDO:0016634 thrombotic disorder due to an acquired coagulation factors defect --> obsolete thrombotic disorder due to an acquired coagulation factors defect
MONDO:0016636 thrombotic disorder due to a constitutional platelet anomaly --> obsolete thrombotic disorder due to a constitutional platelet anomaly
MONDO:0016637 thrombotic disorder due to an acquired platelet anomaly --> obsolete thrombotic disorder due to an acquired platelet anomaly
MONDO:0016768 rare mucosal lichen planus --> obsolete rare mucosal lichen planus
MONDO:0016992 peeling skin syndrome type B --> obsolete peeling skin syndrome type B
MONDO:0017120 other syndrome with a central nervous system malformation as major feature --> obsolete other syndrome with a central nervous system malformation as major feature
MONDO:0017122 genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature --> obsolete genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
MONDO:0017125 oculofaciocardiodental syndrome --> obsolete oculofaciocardiodental syndrome
MONDO:0017142 hemorrhagic disorder due to a qualitative platelet defect --> obsolete hemorrhagic disorder due to a qualitative platelet defect
MONDO:0017159 syndrome with pulmonary hypertension as a major feature --> obsolete syndrome with pulmonary hypertension as a major feature
MONDO:0017166 rare tumor of salivary glands --> obsolete rare tumor of salivary glands
MONDO:0017297 CLIPPERS --> chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids {xref="Orphanet:284448"}
MONDO:0017631 rare tumor of gallbladder and extrahepatic biliary tract --> obsolete rare tumor of gallbladder and extrahepatic biliary tract
MONDO:0017633 rare intoxication due to medical products --> obsolete rare intoxication due to medical products
MONDO:0017637 rare parkinsonian syndrome due to intoxication --> obsolete rare parkinsonian syndrome due to intoxication
MONDO:0017652 rare disease with myoclonus as a major feature --> obsolete rare disease with myoclonus as a major feature
MONDO:0017657 rare paroxysmal movement disorder --> obsolete rare paroxysmal movement disorder
MONDO:0017661 rare parkinsonian syndrome due to genetic neurodegenerative disease --> obsolete rare parkinsonian syndrome due to genetic neurodegenerative disease
MONDO:0017665 rare genetic disease with myoclonus as a major feature --> obsolete rare genetic disease with myoclonus as a major feature
MONDO:0017669 disease with diffuse palmoplantar keratoderma as a major feature --> obsolete disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0017671 autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature --> obsolete autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0017674 disease with focal palmoplantar keratoderma as a major feature --> obsolete disease with focal palmoplantar keratoderma as a major feature
MONDO:0017678 obsolete disease with punctate palmoplantar keratoderma as a major feature --> obsolete obsolete disease with punctate palmoplantar keratoderma as a major feature
MONDO:0017679 obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature --> obsolete obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
MONDO:0017820 obsolete disease with Cushing syndrome as a major feature --> obsolete obsolete disease with Cushing syndrome as a major feature
MONDO:0018033 other immunodeficiency syndromes due to defects in innate immunity --> obsolete other immunodeficiency syndromes due to defects in innate immunity
MONDO:0018041 other immunodeficiency syndrome with predominantly antibody defects --> obsolete other immunodeficiency syndrome with predominantly antibody defects
MONDO:0018235 dysostosis with limb anomaly as a major feature --> obsolete dysostosis with limb anomaly as a major feature
MONDO:0018236 dysostosis with limb and face anomalies as a major feature --> obsolete dysostosis with limb and face anomalies as a major feature
MONDO:0018265 rare disorder with dystonia and other neurologic or systemic manifestation --> obsolete rare disorder with dystonia and other neurologic or systemic manifestation
MONDO:0018285 X-linked congenital disorder of glycosylation with intellectual disability as a major feature --> obsolete X-linked congenital disorder of glycosylation with intellectual disability as a major feature
MONDO:0018286 non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature --> obsolete non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature
MONDO:0018287 congenital disorder of glycosylation with epilepsy as a major feature --> obsolete congenital disorder of glycosylation with epilepsy as a major feature
MONDO:0018290 congenital disorder of glycosylation with cardiac malformation as a major feature --> obsolete congenital disorder of glycosylation with cardiac malformation as a major feature
MONDO:0018294 congenital disorder of glycosylation with nephropathy as a major feature --> obsolete congenital disorder of glycosylation with nephropathy as a major feature
MONDO:0018295 congenital disorder of glycosylation with deafness as a major feature --> obsolete congenital disorder of glycosylation with deafness as a major feature
MONDO:0018377 rare hereditary disease with avascular necrosis --> obsolete rare hereditary disease with avascular necrosis
MONDO:0018386 rare male infertility due to hypothalamic-pituitary-gonadal axis disorder --> obsolete rare male infertility due to hypothalamic-pituitary-gonadal axis disorder
MONDO:0018387 rare male infertility due to adrenal disorder --> obsolete rare male infertility due to adrenal disorder
MONDO:0018388 rare male infertility due to testicular endocrine disorder --> obsolete rare male infertility due to testicular endocrine disorder
MONDO:0018396 rare male fertility disorder with obstructive azoospermia --> obsolete rare male fertility disorder with obstructive azoospermia
MONDO:0018397 female infertility due to hypothalamic-pituitary-gonadal axis disorder --> obsolete female infertility due to hypothalamic-pituitary-gonadal axis disorder
MONDO:0018400 rare female infertility due to an adrenal disorder --> obsolete rare female infertility due to an adrenal disorder
MONDO:0018401 female infertility due to an anomaly of ovarian function --> obsolete female infertility due to an anomaly of ovarian function
MONDO:0018405 rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin --> obsolete rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
MONDO:0018406 rare male infertility due to adrenal disorder of genetic origin --> obsolete rare male infertility due to adrenal disorder of genetic origin
MONDO:0018409 rare genetic disorder with obstructive azoospermia --> obsolete rare genetic disorder with obstructive azoospermia
MONDO:0018411 rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin --> obsolete rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
MONDO:0018412 rare female infertility due to adrenal disorder of genetic origin --> obsolete rare female infertility due to adrenal disorder of genetic origin
MONDO:0018413 female infertility due to an anomaly of ovarian function of genetic origin --> obsolete female infertility due to an anomaly of ovarian function of genetic origin
MONDO:0018455 dysostosis of genetic origin with limb anomaly as a major feature --> obsolete dysostosis of genetic origin with limb anomaly as a major feature
MONDO:0018457 rare genetic bone development disorder --> obsolete rare genetic bone development disorder
MONDO:0018488 rare genetic odontal or periodontal disorder --> obsolete rare genetic odontal or periodontal disorder
MONDO:0018520 rare epithelial tumor of pancreas --> obsolete rare epithelial tumor of pancreas
MONDO:0018530 rare epithelial tumor of liver and intrahepatic biliary tract --> obsolete rare epithelial tumor of liver and intrahepatic biliary tract
MONDO:0018539 rare epithelial tumor of small intestine --> obsolete rare epithelial tumor of small intestine
MONDO:0018719 obsolete rare capillary malformation with associated anomalies --> obsolete obsolete rare capillary malformation with associated anomalies
MONDO:0018721 rare combined vascular malformation --> obsolete rare combined vascular malformation
MONDO:0018723 rare vascular malformation of major vessels --> obsolete rare vascular malformation of major vessels
MONDO:0018730 rare genetic venous malformation --> obsolete rare genetic venous malformation
MONDO:0018753 rare disease with malignant hyperthermia --> obsolete rare disease with malignant hyperthermia
MONDO:0018798 other genetic dermis disorder --> obsolete other genetic dermis disorder
MONDO:0018833 rare idiopathic macular telangiectasia --> obsolete rare idiopathic macular telangiectasia
MONDO:0018880 rare teratologic disease --> obsolete rare teratologic disease
MONDO:0018972 rare epithelial tumor of stomach --> obsolete rare epithelial tumor of stomach
MONDO:0019014 mutilating palmoplantar keratoderma with periorificial keratotic plaques --> obsolete mutilating palmoplantar keratoderma with periorificial keratotic plaques
MONDO:0019038 rare maxillo-facial surgical disease --> obsolete rare maxillo-facial surgical disease
MONDO:0019039 rare hemorrhagic disorder due to a constitutional coagulation factors defect --> obsolete rare hemorrhagic disorder due to a constitutional coagulation factors defect
MONDO:0019061 rare parathyroid disease and phosphocalcic metabolism anomaly --> obsolete rare parathyroid disease and phosphocalcic metabolism anomaly
MONDO:0019097 hemorrhagic disorder due to a constitutional platelet anomaly --> obsolete hemorrhagic disorder due to a constitutional platelet anomaly
MONDO:0019252 other metabolic disease with skin involvement --> obsolete other metabolic disease with skin involvement
MONDO:0019274 other epidermal disorder --> obsolete other epidermal disorder
MONDO:0019275 other genetic epidermal disease --> obsolete other genetic epidermal disease
MONDO:0019304 rare photodermatosis --> obsolete rare photodermatosis
MONDO:0019546 other acquired skin disease --> obsolete other acquired skin disease
MONDO:0019590 rare endocrine growth disease --> obsolete rare endocrine growth disease
MONDO:0019602 other inborn metabolic disease --> obsolete other inborn metabolic disease
MONDO:0019663 short rib-polydactyly syndrome, Saldino-Noonan type --> obsolete short rib-polydactyly syndrome, Saldino-Noonan type
MONDO:0019744 rare renal tubular disease --> obsolete rare renal tubular disease
MONDO:0019748 rare cause of hypertension --> obsolete rare cause of hypertension
MONDO:0019936 rare otorhinolaryngological malformation --> obsolete rare otorhinolaryngological malformation
MONDO:0019937 rare gynecologic or obstetric disease --> obsolete rare gynecologic or obstetric disease
MONDO:0020013 rare odontologic disease --> obsolete rare odontologic disease
MONDO:0020014 rare disease with odontological manifestation --> obsolete rare disease with odontological manifestation
MONDO:0020016 rare neurologic disease with psychiatric involvement --> obsolete rare neurologic disease with psychiatric involvement
MONDO:0020035 rare otorhinolaryngologic tumor --> obsolete rare otorhinolaryngologic tumor
MONDO:0020094 autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature --> obsolete autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0020095 autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature --> obsolete autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature
MONDO:0020097 autosomal recessive disease with focal palmoplantar keratoderma as a major feature --> obsolete autosomal recessive disease with focal palmoplantar keratoderma as a major feature
MONDO:0020104 rare constitutional hemolytic anemia due to an enzyme disorder --> obsolete rare constitutional hemolytic anemia due to an enzyme disorder
MONDO:0020149 rare eye disease due to a differentiation anomaly --> obsolete rare eye disease due to a differentiation anomaly
MONDO:0020150 obsolete rare palpebral, lacrimal system and conjunctival disease --> obsolete obsolete rare palpebral, lacrimal system and conjunctival disease
MONDO:0020152 rare eyelid malformation --> obsolete rare eyelid malformation
MONDO:0020169 rare disorder with ptosis --> obsolete rare disorder with ptosis
MONDO:0020206 rare refraction anomaly --> obsolete rare refraction anomaly
MONDO:0020209 rare hyperopia and astigmatism --> obsolete rare hyperopia and astigmatism
MONDO:0020222 rare disease with glaucoma as a major feature --> obsolete rare disease with glaucoma as a major feature
MONDO:0020223 lens and zonula anomaly --> obsolete lens and zonula anomaly
MONDO:0020251 rare strabismus and restriction syndrome --> obsolete rare strabismus and restriction syndrome
MONDO:0020258 oculomotor apraxia or related oculomotor disease --> obsolete oculomotor apraxia or related oculomotor disease
MONDO:0020484 rare familial disorder with hypertrophic cardiomyopathy --> obsolete rare familial disorder with hypertrophic cardiomyopathy
MONDO:0020671 susceptibility to ischemic stroke --> obsolete susceptibility to ischemic stroke
MONDO:0020737 optic atrophy 10 with or without ataxia, mental retardation, and seizures --> optic atrophy 10 with or without ataxia, intellectual disability, and seizures
MONDO:0020755 heart block --> obsolete heart block
MONDO:0020803 bundle branch block --> obsolete bundle branch block
MONDO:0020846 mental retardation, autosomal recessive 64 --> intellectual disability, autosomal recessive 64
MONDO:0020847 mental retardation, autosomal dominant 58 --> intellectual disability, autosomal dominant 58
MONDO:0021570 Hauptmann-Thannhauser muscular dystrophy --> obsolete Hauptmann-Thannhauser muscular dystrophy
MONDO:0021849 alopecia macular degeneration growth retardation syndome --> alopecia macular degeneration growth retardation syndrome
MONDO:0022676 cataract - glaucoma --> obsolete cataract - glaucoma
MONDO:0022732 chorea minor --> obsolete chorea minor
MONDO:0022778 cleft lip palate mental retardation corneal opacity --> cleft lip palate intellectual disability corneal opacity
MONDO:0022832 congenital heart disease radio ulnar synostosis mental retardation --> congenital heart disease radio ulnar synostosis intellectual disability
MONDO:0022865 corneal dystrophy ichthyosis microcephaly mental retardation --> corneal dystrophy ichthyosis microcephaly intellectual disability
MONDO:0022889 craniostenosis with congenital heart disease mental retardation --> craniostenosis with congenital heart disease intellectual disability
MONDO:0022898 craniosynostosis mental retardation heart defects --> craniosynostosis intellectual disability heart defects
MONDO:0023272 goniodysgenesis mental retardation short stature --> goniodysgenesis intellectual disability short stature
MONDO:0024542 cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1 --> cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
MONDO:0025517 shrimp allergy --> obsolete shrimp allergy
MONDO:0025518 aspirin allergy --> obsolete aspirin allergy
MONDO:0026733 intellectual developmental disorder, x-linked, syndromic, Hackmann-Di Donato type --> intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type
MONDO:0026763 holoprosencephaly 13, x-linked --> holoprosencephaly 13, X-linked
MONDO:0026767 immunodeficiency 74, covid19-related, x-linked --> immunodeficiency 74, covid19-related, X-linked
MONDO:0026768 warfarin sensitivity, x-linked --> warfarin sensitivity, X-linked
MONDO:0028737 biliary atresia disorder --> obsolete biliary atresia disorder
MONDO:0030009 alopecia-mental retardation syndrome 4 --> alopecia-intellectual disability syndrome 4
MONDO:0032605 mental retardation, autosomal recessive 66 --> intellectual disability, autosomal recessive 66
MONDO:0042724 macrocephaly, mental retardation, short stature, spastic paraplegia and cns malformations --> macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations
MONDO:0042726 macrogyria, pseudobulbar palsy and mental retardation --> macrogyria, pseudobulbar palsy and intellectual disability
MONDO:0043139 microcephaly sparse hair mental retardation seizures --> microcephaly sparse hair intellectual disability seizures
MONDO:0044313 mental retardation, autosomal recessive 60 --> intellectual disability, autosomal recessive 60
MONDO:0044636 rare hyperkinetic movement disorder --> obsolete rare hyperkinetic movement disorder
MONDO:0044680 short rib-polydactyly syndrome type 5 --> obsolete short rib-polydactyly syndrome type 5
MONDO:0044808 early onset primary dystonia --> obsolete early onset primary dystonia
MONDO:0049222 intellectual disability, x-linked 107 --> intellectual disability, X-linked 107
MONDO:0054837 mental retardation, autosomal dominant 57 --> intellectual disability, autosomal dominant 57
MONDO:0060649 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies --> obsolete short stature, facial dysmorp...

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v2021-04-07

New Classes

Obsoletions

Renaming