v2021-09-01
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5118 commits
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since this release
New Classes
- MONDO:0025708 megacystis-microcolon-intestinal hypoperistalsis syndrome 2
- MONDO:0035349 localized dystrophic epidermolysis bullosa
- MONDO:0035354 IgG4-related systemic disease
- MONDO:0035357 portosinusoidal vascular disease
- MONDO:0035362 TRIM22-related inflammatory bowel disease
- MONDO:0035363 IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome
- MONDO:0035369 MTHFS-related developmental delay-microcephaly-short stature-epilepsy syndrome
- MONDO:0035370 ALPI-related inflammatory bowel disease
- MONDO:0035375 multisystem inflammatory syndrome in children and adults
- MONDO:0035398 hypomyelination of early myelinating structures
- MONDO:0100041 secondary trimethylaminuria
- MONDO:0100044 acrofrontofacionasal dysostosis 1
- MONDO:0550003 SEC61B-related polycystic liver disease
- MONDO:0700085 pentasomy
- MONDO:0700086 uniparental disomy
- MONDO:0700087 Usher syndrome type 1B
- MONDO:0700088 paroxysmal nonkinesigenic dyskinesia
- MONDO:0700089 paroxysmal nonkinesigenic dyskinesia 1
- MONDO:0700090 epilepsy, familial temporal lobe, 1
- MONDO:0800001 delayed sleep phase syndrome, susceptibility to
Obsoletions
- MONDO:0004424 familial glomangioma --> obsolete familial glomangioma
- MONDO:0005261 pervasive developmental disorder - not otherwise specified --> obsolete pervasive developmental disorder - not otherwise specified
- MONDO:0005442 type 1 diabetes nephropathy --> obsolete type 1 diabetes nephropathy
- MONDO:0005443 type 2 diabetes nephropathy --> obsolete type 2 diabetes nephropathy
- MONDO:0007326 paroxysmal nonkinesigenic dyskinesia 1 --> obsolete paroxysmal nonkinesigenic dyskinesia 1
- MONDO:0015119 bronchopulmonary tumor --> obsolete bronchopulmonary tumor
- MONDO:0015989 congenital valvular dysplasia --> obsolete congenital valvular dysplasia
- MONDO:0016254 rare variants of adenocarcinoma of the corpus uteri --> obsolete rare variants of adenocarcinoma of the corpus uteri
- MONDO:0016629 hemorrhagic disorder due to a platelet anomaly --> obsolete hemorrhagic disorder due to a platelet anomaly
- MONDO:0016632 thrombotic disorder due to a coagulation factors defect --> obsolete thrombotic disorder due to a coagulation factors defect
- MONDO:0016635 thrombotic disorder due to a platelet anomaly --> obsolete thrombotic disorder due to a platelet anomaly
- MONDO:0016767 cutaneous lichen planus --> obsolete cutaneous lichen planus
- MONDO:0017141 hemorrhagic disorder due to a constitutional thrombocytopenia --> obsolete hemorrhagic disorder due to a constitutional thrombocytopenia
- MONDO:0017663 inherited tremor disorder --> obsolete inherited tremor disorder
- MONDO:0018729 genetic vascular tumor --> obsolete genetic vascular tumor
- MONDO:0019183 inherited odontologic disease --> obsolete inherited odontologic disease
- MONDO:0020092 rare idiopathic male infertility --> obsolete rare idiopathic male infertility
- MONDO:0021720 fetal alcohol spectrum disorders --> obsolete fetal alcohol spectrum disorders
Renaming
- MONDO:0004424 familial glomangioma --> obsolete familial glomangioma
- MONDO:0005261 pervasive developmental disorder - not otherwise specified --> obsolete pervasive developmental disorder - not otherwise specified
- MONDO:0005442 type 1 diabetes nephropathy --> obsolete type 1 diabetes nephropathy
- MONDO:0005443 type 2 diabetes nephropathy --> obsolete type 2 diabetes nephropathy
- MONDO:0005554 rheumatologic disorder --> rheumatic disorder
- MONDO:0007326 paroxysmal nonkinesigenic dyskinesia 1 --> obsolete paroxysmal nonkinesigenic dyskinesia 1
- MONDO:0008757 alopecia universalis --> alopecia universalis congenita
- MONDO:0009402 hypertelorism-hypospadias-polysyndactyly syndrome --> acrofrontofacionasal dysostosis 2
- MONDO:0014175 mitochondrial DNA depletion syndrome 12 --> mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive
- MONDO:0014243 Prader-Willi syndrome due to point mutation --> Schaaf-Yang syndrome
- MONDO:0014959 mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant --> mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant
- MONDO:0015119 bronchopulmonary tumor --> obsolete bronchopulmonary tumor
- MONDO:0015989 congenital valvular dysplasia --> obsolete congenital valvular dysplasia
- MONDO:0016254 rare variants of adenocarcinoma of the corpus uteri --> obsolete rare variants of adenocarcinoma of the corpus uteri
- MONDO:0016629 hemorrhagic disorder due to a platelet anomaly --> obsolete hemorrhagic disorder due to a platelet anomaly
- MONDO:0016632 thrombotic disorder due to a coagulation factors defect --> obsolete thrombotic disorder due to a coagulation factors defect
- MONDO:0016635 thrombotic disorder due to a platelet anomaly --> obsolete thrombotic disorder due to a platelet anomaly
- MONDO:0016767 cutaneous lichen planus --> obsolete cutaneous lichen planus
- MONDO:0017141 hemorrhagic disorder due to a constitutional thrombocytopenia --> obsolete hemorrhagic disorder due to a constitutional thrombocytopenia
- MONDO:0017663 inherited tremor disorder --> obsolete inherited tremor disorder
- MONDO:0018729 genetic vascular tumor --> obsolete genetic vascular tumor
- MONDO:0019183 inherited odontologic disease --> obsolete inherited odontologic disease
- MONDO:0020092 rare idiopathic male infertility --> obsolete rare idiopathic male infertility
- MONDO:0020726 medullary cystic kidney disease 1 --> tubulointerstitial kidney disease, autosomal dominant, 2
- MONDO:0021720 fetal alcohol spectrum disorders --> obsolete fetal alcohol spectrum disorders
- MONDO:0023007 drachtman weinblatt sitarz syndrome --> Drachtman Weinblatt Sitarz syndrome
- MONDO:0029141 usher syndrome, type 4 --> Usher syndrome, type 4
- MONDO:0030899 oculocutaneous albinism, type 8 --> oculocutaneous albinism type 8
- MONDO:0100232 'psoriatic arthritis, susceptibility to --> psoriatic arthritis, susceptibility to
- MONDO:0700066 myopathy caused by mutation in FKRP --> myopathy caused by varation in FKRP
- MONDO:0700067 myopathy caused by mutation in FKTN --> myopathy caused by varation in FKTN
- MONDO:0700068 myopathy caused by mutation in POMGNT1 --> myopathy caused by varation in POMGNT1
- MONDO:0700069 myopathy caused by mutation in POMGNT2 --> myopathy caused by varation in POMGNT2
- MONDO:0700070 myopathy caused by mutation in POMT1 --> myopathy caused by varation in POMT1
- MONDO:0700071 myopathy caused by mutation in POMT2 {xref="MONDO:patterns/disease_series_by_gene"} --> myopathy caused by varation in POMT2
- MONDO:0700075 congenital muscular dystrophy caused by mutation in POMGNT2 --> congenital muscular dystrophy caused by varation in POMGNT2
- MONDO:0700084 myopathy caused by mutation in GMPPB --> myopathy caused by varation in GMPPB