Skip to content

v2024-07-02
Compare
Choose a tag to compare
@sabrinatoro sabrinatoro released this 02 Jul 22:35
· 385 commits to master since this release
v2024-07-02
b204716
This commit was created on GitHub.com and signed with GitHub’s verified signature.
GPG key ID: B5690EEEBB952194
Verified
Learn about vigilant mode.

Overview:

  • Number of new terms: 641
  • Number of changed labels: 2
  • Number of changed definitions: 3
  • Number obsoleted terms: 5
  • Number of new obsoletion candidates: 352
  • Number of terms who were previously candidate for obsoletion and are now not anymore: 0

New terms

Mondo ID Label Definition
MONDO:0968990 genetic central precocious puberty in male
MONDO:0968991 non-genetic central precocious puberty in male
MONDO:0970943 spermatogenic failure, x-linked, 8
MONDO:0970944 Leigh syndrome, mitochondrial
MONDO:0970945 developmental and epileptic encephalopathy 116
MONDO:0970950 Rothmund-Thomson syndrome, type 4
MONDO:0970951 El Hayek-Chahrour neurodevelopmental disorder
MONDO:0970952 spermatogenic failure 91
MONDO:0970957 terminal extramedullary conus spinal cord lipoma A rare form of extramedullary conus region spinal cord lipoma characterized by its location, extending from the poorly delineated tip of the conus.
MONDO:0970958 transitional extramedullary conus spinal cord lipoma A rare form of extramedullary conus region spinal cord lipoma characterized by a location at the posterior surface of the conus and its tip. i.e-\transitional" between posterior and terminal conus region spinal cord lipoma."
MONDO:0970959 posterior extramedullary conus spinal cord lipoma A rare form of conus region spinal cord lipoma characterized by its location where the interface between the lipoma and the spinal cord is strictcly above the level of the tip of the conus. The tip of the conus is readily delineated.
MONDO:0970960 lipomatous non-saccular limited dorsal myeloschisis A rare non-saccular limited dorsal myeloschisis histologically characterized by skin tissue with a jagged depression of squamous epithelium continued to subcutaneous mature adipose tissue with loose connective tissue. GFAP-immunopositive glial cells are embedded in the subcutaneous lipoma. The extradural and intradural stalk have cord-like fibrocollagenous tissue containing adipose tissue, peripheral nerve fibers, clusters of melanocytes, and skeletal muscle fibers.
MONDO:0970961 fibroneural non-saccular limited dorsal myeloschisis A rare non-saccular limited dorsal myeloschisis, in which the stalk histology is characterized by skin tissue with dermo-epidermal epithelium in continuity with a subcutaneous fibrocollagenous tract containing various ectopic tissues.
MONDO:0970962 terminal myelocystocele A rare closed spinal dysraphism characterized by a myelocystocele at the termination of the spinal cord. It may be an isolated anomaly or be associated with other defects, including sacral agenesis, anorectal and genitourinary anomalies. The conus is not identifiable. The myelocystocele sac may have a significant lipomatous component (terminal lipomyelocystocele).
MONDO:0970963 saccular limited dorsal myeloschisis A rare form of limited dorsal myeloschisis (LDM), characterized by the stalk attached to the apex of a fully epithelialized meningocele. Chiari II malformation is not present.
MONDO:0970964 myelic limited dorsal malformation A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulated spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized.
MONDO:0970993 immunodeficiency 119
MONDO:0970994 immunodeficiency 120
MONDO:0970995 premature ovarian failure 24
MONDO:0970998 auroneurodental syndrome
MONDO:0970999 spermatogenic failure 92
MONDO:0971000 spermatogenic failure 93
MONDO:0971001 immunodeficiency 121 with autoinflammation
MONDO:0971002 spermatogenic failure 94
MONDO:0971004 amyloidosis, hereditary systemic 1
MONDO:0971005 MHC class II deficiency 1
MONDO:0971006 MHC class I deficiency 1
MONDO:0971007 neuroocular syndrome 1
MONDO:0971008 amyloidosis, hereditary systemic 3
MONDO:0971009 amyloidosis, hereditary systemic 5
MONDO:0971010 amyloidosis, hereditary systemic 6
MONDO:0971011 MHC class I deficiency 2
MONDO:0971012 MHC class I deficiency 3
MONDO:0971013 MHC class II deficiency 2
MONDO:0971014 MHC class II deficiency 3
MONDO:0971015 MHC class II deficiency 4
MONDO:0971016 MHC class II deficiency 5
MONDO:1011400 pituitary-dependent hyperadrenocorticism, non-human animal Pituitary-dependent hyperadrenocorticism that occurs in non-human animals.
MONDO:1011401 type 1 diabetes mellitus, non-human animal Type 1 diabetes mellitus that occurs in non-human animals.
MONDO:1011402 type 2 diabetes mellitus, non-human animal Type 2 diabetes mellitus that occurs in non-human animals.
MONDO:1011403 hyperadrenocorticism, non-human animal Hyperadrenocorticism that occurs in non-human animals.
MONDO:1011404 metabolic syndrome, non-human animal Metabolic syndrome that occurs in non-human animals.
MONDO:1011405 Diamond-Blackfan anemia, non-human animal Diamond-Blackfan anemia that occurs in non-human animals.
MONDO:1011406 autoimmune hemolytic anemia, non-human animal Autoimmune hemolytic anemia that occurs in non-human animals.
MONDO:1011407 nonspherocytic hemolytic anemia, non-human animal Nonspherocytic hemolytic anemia that occurs in non-human animals.
MONDO:1011408 hemophilia A, non-human animal Hemophilia A that occurs in non-human animals.
MONDO:1011409 portosystemic shunt, non-human animal Portosystemic shunt that occurs in non-human animals.
MONDO:1011410 vitamin-K-dependent blood coagulation factors deficiency, non-human animal Vitamin-K-Dependent blood coagulation factors deficiency that occurs in non-human animals.
MONDO:1011411 Von Willebrand disease, non-human animal Von Willebrand disease that occurs in non-human animals.
MONDO:1011412 methemoglobinemia, non-human animal Methemoglobinemia that occurs in non-human animals.
MONDO:1011413 paroxysmal nocturnal hemoglobinuria, non-human animal Paroxysmal nocturnal hemoglobinuria that occurs in non-human animals.
MONDO:1011414 vestibular disease, non-human animal Vestibular disease that occurs in non-human animals.
MONDO:1011415 amyloidosis, non-human animal Amyloidosis that occurs in non-human animals.
MONDO:1011416 calcinosis circumscripta, non-human animal Calcinosis circumscripta that occurs in non-human animals.
MONDO:1011417 hypertriglyceridemia, non-human animal Hypertriglyceridemia that occurs in non-human animals.
MONDO:1011418 porphyria, non-human animal Porphyria that occurs in non-human animals.
MONDO:1011419 glycogen storage disease, non-human animal Glycogen storage disease that occurs in non-human animals.
MONDO:1011420 hyperhomocysteinemia, non-human animal Hyperhomocysteinemia that occurs in non-human animals.
MONDO:1011421 complement component 3 deficiency, non-human animal Complement component 3 deficiency that occurs in non-human animals.
MONDO:1011422 severe combined immunodeficiency disease, non-human animal Severe combined immunodeficiency disease that occurs in non-human animals.
MONDO:1011423 Complement component 6 deficiency, non-human animal Complement component 6 deficiency that occurs in non-human animals.
MONDO:1011424 Complement component 2 deficiency, non-human animal Complement component 2 deficiency that occurs in non-human animals.
MONDO:1011425 Ehlers-Danlos syndrome, non-human animal Ehlers-Danlos syndrome that occurs in non-human animals.
MONDO:1011426 junctionalis epidermolysis bullosa , non-human animal Junctionalis epidermolysis bullosa that occurs in non-human animals.
MONDO:1011427 ichthyosis, non-human animal Ichthyosis that occurs in non-human animals.
MONDO:1011428 epidermolysis bullosa simplex, non-human animal Epidermolysis bullosa simplex that occurs in non-human animals.
MONDO:1011429 hepatic lipidosis, non-human animal Hepatic lipidosis that occurs in non-human animals.
MONDO:1011430 neuronal ceroid lipofuscinosis, non-human animal Neuronal ceroid lipofuscinosis that occurs in non-human animals.
MONDO:1011431 Gaucher disease, non-human animal Gaucher disease that occurs in non-human animals.
MONDO:1011432 beta-mannosidosis, non-human animal Beta-mannosidosis that occurs in non-human animals.
MONDO:1011433 hyperkalemic periodic paralysis, non-human animal Hyperkalemic periodic paralysis that occurs in non-human animals.
MONDO:1011434 hypokalaemic periodic paralysis, non-human animal Hypokalaemic periodic paralysis that occurs in non-human animals.
MONDO:1011435 Becker type muscular dystrophy, non-human animal Becker type muscular dystrophy that occurs in non-human animals.
MONDO:1011436 histiocytosis, non-human animal Histiocytosis that occurs in non-human animals.
MONDO:1011437 neurofibromatosis, non-human animal Neurofibromatosis that occurs in non-human animals.
MONDO:1011438 nephroma, non-human animal Nephroma that occurs in non-human animals.
MONDO:1011439 Wilms tumor, non-human animal Wilms tumour that occurs in non-human animals.
MONDO:1011440 gastrointestinal stromal tumour, non-human animal Gastrointestinal stromal tumour that occurs in non-human animals.
MONDO:1011441 mast cell tumor, non-human animal Mast cell tumor that occurs in non-human animals.
MONDO:1011442 enteropathy-associated T cell lymphoma, non-human animal Enteropathy-associated T cell lymphoma that occurs in non-human animals.
MONDO:1011443 Alzheimer disease, non-human animal Alzheimer disease that occurs in non-human animals.
MONDO:1011444 neuroaxonal dystrophy, non-human animal Neuroaxonal dystrophy that occurs in non-human animals.
MONDO:1011445 fibrocartilaginous embolic myelopathy, non-human animal Fibrocartilaginous embolic myelopathy that occurs in non-human animals.
MONDO:1011446 medium-chain acyl-CoA dehydrogenase deficiency, non-human animal Medium-Chain acyl-CoA dehydrogenase deficiency that occurs in non-human animals.
MONDO:1011447 Waardenburg syndrome, non-human animal Waardenburg syndrome that occurs in non-human animals.
MONDO:1011448 Fanconi syndrome, non-human animal Fanconi syndrome that occurs in non-human animals.
MONDO:1011449 immunoglobulin A glomerulonephropathy, non-human animal Immunoglobulin A glomerulonephropathy that occurs in non-human animals.
MONDO:1011450 xanthinuria, non-human animal Xanthinuria that occurs in non-human animals.
MONDO:1011451 idiopathic pulmonary fibrosis, non-human animal Idiopathic pulmonary fibrosis that occurs in non-human animals.
MONDO:1011452 intervertebral disc disease, non-human animal Intervertebral disc disease that occurs in non-human animals.
MONDO:1011453 Legg-Calvé-Perthes disease, non-human animal Legg-Calvé-Perthes disease that occurs in non-human animals.
MONDO:1011454 osteogenesis imperfecta, non-human animal Osteogenesis imperfecta that occurs in non-human animals.
MONDO:1011455 arthrogryposis multiplex congenita, non-human animal Arthrogryposis multiplex congenita that occurs in non-human animals.
MONDO:1011456 rickets, non-human animal Rickets that occurs in non-human animals.
MONDO:1011457 glaucoma, non-human animal Glaucoma that occurs in non-human animals.
MONDO:1011458 glaucoma, primary closed-angle, non-human animal Glaucoma, primary closed-angle that occurs in non-human animals.
MONDO:1011459 ligneous membranitis, non-human animal Ligneous membranitis that occurs in non-human animals.
MONDO:1011460 Alzheimer disease, degu Alzheimer disease that occurs in degu.
MONDO:1011461 Alzheimer disease, dog Alzheimer disease that occurs in dog.
MONDO:1011462 Alzheimer disease, domestic cat Alzheimer disease that occurs in domestic cat.
MONDO:1011463 Alzheimer disease, sheep Alzheimer disease that occurs in sheep.
MONDO:1011464 amyloidosis, black-footed cat Amyloidosis that occurs in black-footed cat.
MONDO:1011465 amyloidosis, black-footed ferret Amyloidosis that occurs in black-footed ferret.
MONDO:1011466 amyloidosis, chicken Amyloidosis that occurs in chicken.
MONDO:1011467 amyloidosis, dog Amyloidosis that occurs in dog.
MONDO:1011468 amyloidosis, domestic cat Amyloidosis that occurs in domestic cat.
MONDO:1011469 amyloidosis, domestic goose Amyloidosis that occurs in domestic goose.
MONDO:1011470 amyloidosis, ducks Amyloidosis that occurs in ducks.
MONDO:1011471 amyloidosis, goat Amyloidosis that occurs in goat.
MONDO:1011472 amyloidosis, golden hamster Amyloidosis that occurs in golden hamster.
MONDO:1011473 amyloidosis, Japanese quail Amyloidosis that occurs in Japanese quail.
MONDO:1011474 arthrogryposis multiplex congenita, cattle Arthrogryposis multiplex congenita that occurs in cattle.
MONDO:1011475 arthrogryposis multiplex congenita, pig Arthrogryposis multiplex congenita that occurs in pig.
MONDO:1011476 arthrogryposis multiplex congenita, sheep Arthrogryposis multiplex congenita that occurs in sheep.
MONDO:1011477 autoimmune hemolytic anemia, dog Autoimmune hemolytic anemia that occurs in dog.
MONDO:1011478 autoimmune hemolytic anemia, domestic cat Autoimmune hemolytic anemia that occurs in domestic cat.
MONDO:1011479 Becker type muscular dystrophy, dog Becker type muscular dystrophy that occurs in dog.
MONDO:1011480 Becker type muscular dystrophy, pig Becker type muscular dystrophy that occurs in pig.
MONDO:1011481 beta-mannosidosis, cattle Beta-mannosidosis that occurs in cattle.
MONDO:1011482 beta-mannosidosis, dog Beta-mannosidosis that occurs in dog.
MONDO:1011483 beta-mannosidosis, goat Beta-mannosidosis that occurs in goat.
MONDO:1011484 beta-mannosidosis, springbok Beta-mannosidosis that occurs in springbok.
MONDO:1011485 calcinosis circumscripta, dog Calcinosis circumscripta that occurs in dog.
MONDO:1011486 complement component 2 deficiency, domestic guinea pig Complement component 2 deficiency that occurs in domestic guinea pig.
MONDO:1011487 complement component 3 deficiency, dog Complement component 3 deficiency that occurs in dog.
MONDO:1011488 complement component 3 deficiency, domestic guinea pig Complement component 3 deficiency that occurs in domestic guinea pig.
MONDO:1011489 complement component 3 deficiency, rabbit Complement component 3 deficiency that occurs in rabbit.
MONDO:1011490 complement component 6 deficiency, rabbit Complement component 6 deficiency that occurs in rabbit.
MONDO:1011491 Diamond-Blackfan anemia, dog Diamond-Blackfan anemia that occurs in dog.
MONDO:1011492 Ehlers-Danlos syndrome, American mink Ehlers-Danlos syndrome that occurs in American mink.
MONDO:1011493 Ehlers-Danlos syndrome, dog Ehlers-Danlos syndrome that occurs in dog.
MONDO:1011494 Ehlers-Danlos syndrome, domestic cat Ehlers-Danlos syndrome that occurs in domestic cat.
MONDO:1011495 Ehlers-Danlos syndrome, horse Ehlers-Danlos syndrome that occurs in horse.
MONDO:1011496 Ehlers-Danlos syndrome, rabbit Ehlers-Danlos syndrome that occurs in rabbit.
MONDO:1011497 Ehlers-Danlos syndrome, sheep Ehlers-Danlos syndrome that occurs in sheep.
MONDO:1011498 enteropathy-associated T cell lymphoma, domestic cat Enteropathy-associated T cell lymphoma that occurs in domestic cat.
MONDO:1011499 epidermolysis bullosa simplex, cattle Epidermolysis bullosa simplex that occurs in cattle.
MONDO:1011500 epidermolysis bullosa simplex, dog Epidermolysis bullosa simplex that occurs in dog.
MONDO:1011501 epidermolysis bullosa simplex, water buffalo Epidermolysis bullosa simplex that occurs in water buffalo.
MONDO:1011502 Fanconi syndrome, cattle Fanconi syndrome that occurs in cattle.
MONDO:1011503 Fanconi syndrome, dog Fanconi syndrome that occurs in dog.
MONDO:1011504 Fanconi syndrome, horse Fanconi syndrome that occurs in horse.
MONDO:1011505 fibrocartilaginous embolic myelopathy, horse Fibrocartilaginous embolic myelopathy that occurs in horse.
MONDO:1011507 Gaucher disease, dog Gaucher disease that occurs in dog.
MONDO:1011508 Gaucher disease, pig Gaucher disease that occurs in pig.
MONDO:1011509 Gaucher disease, sheep Gaucher disease that occurs in sheep.
MONDO:1011510 glaucoma, dog Glaucoma that occurs in dog.
MONDO:1011511 glaucoma, domestic cat Glaucoma that occurs in domestic cat.
MONDO:1011512 glaucoma, horse Glaucoma that occurs in horse.
MONDO:1011513 glaucoma, Japanese quail Glaucoma that occurs in Japanese quail.
MONDO:1011514 glaucoma, owls Glaucoma that occurs in owls.
MONDO:1011515 glaucoma, primary closed-angle, dog Glaucoma, primary closed-angle that occurs in dog.
MONDO:1011516 glaucoma, rabbit Glaucoma that occurs in rabbit.
MONDO:1011517 glaucoma, Rhesus monkey Glaucoma that occurs in Rhesus monkey.
MONDO:1011518 glycogen storage disease, ring-tailed coati Glycogen storage disease that occurs in ring-tailed coati.
MONDO:1011519 hemophilia A, cattle Hemophilia A that occurs in cattle.
MONDO:1011520 hemophilia A, crab-eating macaque Hemophilia A that occurs in crab-eating macaque.
MONDO:1011521 hemophilia A, dog Hemophilia A that occurs in dog.
MONDO:1011522 hemophilia A, domestic cat Hemophilia A that occurs in domestic cat.
MONDO:1011523 hemophilia A, horse Hemophilia A that occurs in horse.
MONDO:1011524 hemophilia A, pig Hemophilia A that occurs in pig.
MONDO:1011525 hemophilia A, sheep Hemophilia A that occurs in sheep.
MONDO:1011526 hepatic lipidosis, cattle Hepatic lipidosis that occurs in cattle.
MONDO:1011527 hepatic lipidosis, domestic cat Hepatic lipidosis that occurs in domestic cat.
MONDO:1011528 histiocytosis, cattle Histiocytosis that occurs in cattle.
MONDO:1011529 histiocytosis, pig Histiocytosis that occurs in pig.
MONDO:1011530 hyperadrenocorticism, dog Hyperadrenocorticism that occurs in dog.
MONDO:1011531 hyperadrenocorticism, domestic cat Hyperadrenocorticism that occurs in domestic cat.
MONDO:1011532 hyperadrenocorticism, domestic ferret Hyperadrenocorticism that occurs in domestic ferret.
MONDO:1011533 hyperadrenocorticism, golden hamster Hyperadrenocorticism that occurs in golden hamster.
MONDO:1011534 hyperadrenocorticism, horse Hyperadrenocorticism that occurs in horse.
MONDO:1011535 hyperhomocysteinemia, dog Hyperhomocysteinemia that occurs in dog.
MONDO:1011536 hyperkalemic periodic paralysis, horse Hyperkalemic periodic paralysis that occurs in horse.
MONDO:1011537 hypertriglyceridemia, dog Hypertriglyceridemia that occurs in dog.
MONDO:1011538 hypertriglyceridemia, domestic cat Hypertriglyceridemia that occurs in domestic cat.
MONDO:1011539 hypokalaemic periodic paralysis, domestic cat Hypokalaemic periodic paralysis that occurs in domestic cat.
MONDO:1011540 hypokalaemic periodic paralysis, lion Hypokalaemic periodic paralysis that occurs in lion.
MONDO:1011541 ichthyosis, cattle Ichthyosis that occurs in cattle.
MONDO:1011542 ichthyosis, greater kudu Ichthyosis that occurs in greater kudu.
MONDO:1011543 idiopathic pulmonary fibrosis, dog Idiopathic pulmonary fibrosis that occurs in dog.
MONDO:1011544 idiopathic pulmonary fibrosis, domestic cat Idiopathic pulmonary fibrosis that occurs in domestic cat.
MONDO:1011545 immunoglobulin A glomerulonephropathy, dog Immunoglobulin A glomerulonephropathy that occurs in dog.
MONDO:1011546 intervertebral disc disease, dog Intervertebral disc disease that occurs in dog.
MONDO:1011547 junctionalis epidermolysis bullosa, cattle Junctionalis epidermolysis bullosa that occurs in cattle.
MONDO:1011548 junctionalis epidermolysis bullosa, dog Junctionalis epidermolysis bullosa that occurs in dog.
MONDO:1011549 junctionalis epidermolysis bullosa, domestic cat Junctionalis epidermolysis bullosa that occurs in domestic cat.
MONDO:1011550 Legg-Calvé-Perthes disease, dog Legg-Calvé-Perthes disease that occurs in dog.
MONDO:1011551 Legg-Calvé-Perthes disease, goat Legg-Calvé-Perthes disease that occurs in goat.
MONDO:1011552 Legg-Calvé-Perthes disease, lesser panda Legg-Calvé-Perthes disease that occurs in lesser panda.
MONDO:1011553 Legg-Calvé-Perthes disease, Rhesus monkey Legg-Calvé-Perthes disease that occurs in Rhesus monkey.
MONDO:1011554 ligneous membranitis, dog Ligneous membranitis that occurs in dog.
MONDO:1011555 mast cell tumor, dog Mast cell tumor that occurs in dog.
MONDO:1011556 medium-chain acyl-CoA dehydrogenase deficiency, dog Medium-chain acyl-CoA dehydrogenase deficiency that occurs in dog.
MONDO:1011557 metabolic syndrome, horse Metabolic syndrome that occurs in horse.
MONDO:1011558 metabolic syndrome, pig Metabolic syndrome that occurs in pig.
MONDO:1011559 methemoglobinemia, domestic cat Methemoglobinemia that occurs in domestic cat.
MONDO:1011560 nephroma, ducks Nephroma that occurs in ducks.
MONDO:1011561 neuroaxonal dystrophy, dog Neuroaxonal dystrophy that occurs in dog.
MONDO:1011562 neuroaxonal dystrophy, domestic cat Neuroaxonal dystrophy that occurs in domestic cat.
MONDO:1011563 neuroaxonal dystrophy, horse Neuroaxonal dystrophy that occurs in horse.
MONDO:1011564 neuroaxonal dystrophy, rabbit Neuroaxonal dystrophy that occurs in rabbit.
MONDO:1011565 neuroaxonal dystrophy, sheep Neuroaxonal dystrophy that occurs in sheep.
MONDO:1011566 neurofibromatosis, cattle Neurofibromatosis that occurs in cattle.
MONDO:1011567 neurofibromatosis, teleost fishes Neurofibromatosis that occurs in teleost fishes.
MONDO:1011568 neuronal ceroid lipofuscinosis, cattle Neuronal ceroid lipofuscinosis that occurs in cattle.
MONDO:1011569 neuronal ceroid lipofuscinosis, crab-eating macaque Neuronal ceroid lipofuscinosis that occurs in crab-eating macaque.
MONDO:1011570 neuronal ceroid lipofuscinosis, dog Neuronal ceroid lipofuscinosis that occurs in dog.
MONDO:1011571 neuronal ceroid lipofuscinosis, domestic cat Neuronal ceroid lipofuscinosis that occurs in domestic cat.
MONDO:1011572 neuronal ceroid lipofuscinosis, domestic ferret Neuronal ceroid lipofuscinosis that occurs in domestic ferret.
MONDO:1011573 neuronal ceroid lipofuscinosis, goat Neuronal ceroid lipofuscinosis that occurs in goat.
MONDO:1011574 neuronal ceroid lipofuscinosis, horse Neuronal ceroid lipofuscinosis that occurs in horse.
MONDO:1011575 neuronal ceroid lipofuscinosis, mallard Neuronal ceroid lipofuscinosis that occurs in mallard.
MONDO:1011576 neuronal ceroid lipofuscinosis, peach-faced lovebird Neuronal ceroid lipofuscinosis that occurs in peach-faced lovebird.
MONDO:1011577 neuronal ceroid lipofuscinosis, pig Neuronal ceroid lipofuscinosis that occurs in pig.
MONDO:1011578 neuronal ceroid lipofuscinosis, sheep Neuronal ceroid lipofuscinosis that occurs in sheep.
MONDO:1011579 nonspherocytic hemolytic anemia, dog Nonspherocytic hemolytic anemia that occurs in dog.
MONDO:1011580 osteogenesis imperfecta, cattle Osteogenesis imperfecta that occurs in cattle.
MONDO:1011581 osteogenesis imperfecta, dog Osteogenesis imperfecta that occurs in dog.
MONDO:1011582 osteogenesis imperfecta, domestic cat Osteogenesis imperfecta that occurs in domestic cat.
MONDO:1011583 osteogenesis imperfecta, sheep Osteogenesis imperfecta that occurs in sheep.
MONDO:1011584 paroxysmal nocturnal hemoglobinuria, Rhesus monkey Paroxysmal nocturnal hemoglobinuria that occurs in Rhesus monkey.
MONDO:1011585 pituitary-dependent hyperadrenocorticism, dog Pituitary-dependent hyperadrenocorticism that occurs in dog.
MONDO:1011586 pituitary-dependent hyperadrenocorticism, domestic cat Pituitary-dependent hyperadrenocorticism that occurs in domestic cat.
MONDO:1011587 porphyria, domestic cat Porphyria that occurs in domestic cat.
MONDO:1011588 porphyria, pig Porphyria that occurs in pig.
MONDO:1011589 portosystemic shunt, cattle Portosystemic shunt that occurs in cattle.
MONDO:1011590 portosystemic shunt, dog Portosystemic shunt that occurs in dog.
MONDO:1011591 portosystemic shunt, domestic cat Portosystemic shunt that occurs in domestic cat.
MONDO:1011592 portosystemic shunt, horse Portosystemic shunt that occurs in horse.
MONDO:1011593 portosystemic shunt, pig Portosystemic shunt that occurs in pig.
MONDO:1011594 rickets, horse Rickets that occurs in horse.
MONDO:1011595 rickets, pig Rickets that occurs in pig.
MONDO:1011596 severe combined immunodeficiency disease, dog Severe combined immunodeficiency disease that occurs in dog.
MONDO:1011597 severe combined immunodeficiency disease, horse Severe combined immunodeficiency disease that occurs in horse.
MONDO:1011598 type 1 diabetes mellitus, cattle Type 1 diabetes mellitus that occurs in cattle.
MONDO:1011599 type 1 diabetes mellitus, chimpanzee Type 1 diabetes mellitus that occurs in chimpanzee.
MONDO:1011600 type 1 diabetes mellitus, domestic cat Type 1 diabetes mellitus that occurs in domestic cat.
MONDO:1011601 type 1 diabetes mellitus, domestic guinea pig Type 1 diabetes mellitus that occurs in domestic guinea pig.
MONDO:1011602 type 2 diabetes mellitus, Chinese hamster Type 2 diabetes mellitus that occurs in Chinese hamster.
MONDO:1011603 type 2 diabetes mellitus, crab-eating macaque Type 2 diabetes mellitus that occurs in crab-eating macaque.
MONDO:1011604 type 2 diabetes mellitus, domestic cat Type 2 diabetes mellitus that occurs in domestic cat.
MONDO:1011605 type 2 diabetes mellitus, pig Type 2 diabetes mellitus that occurs in pig.
MONDO:1011606 vestibular disease, dog Vestibular disease that occurs in dog.
MONDO:1011607 vestibular disease, Sumatran tiger Vestibular disease that occurs in Sumatran tiger.
MONDO:1011608 vitamin-K-dependent blood coagulation factors deficiency, dog Vitamin-K-dependent blood coagulation factors deficiency that occurs in dog.
MONDO:1011609 vitamin-K-dependent blood coagulation factors deficiency, domestic cat Vitamin-K-dependent blood coagulation factors deficiency that occurs in domestic cat.
MONDO:1011610 vitamin-K-dependent blood coagulation factors deficiency, sheep Vitamin-K-dependent blood coagulation factors deficiency that occurs in sheep.
MONDO:1011611 Von Willebrand disease, cattle Von Willebrand disease that occurs in cattle.
MONDO:1011612 Von Willebrand disease, dog Von Willebrand disease that occurs in dog.
MONDO:1011613 Von Willebrand disease, domestic cat Von Willebrand disease that occurs in domestic cat.
MONDO:1011614 Von Willebrand disease, horse Von Willebrand disease that occurs in horse.
MONDO:1011615 Von Willebrand disease, pig Von Willebrand disease that occurs in pig.
MONDO:1011616 Von Willebrand disease, rabbit Von Willebrand disease that occurs in rabbit.
MONDO:1011617 Waardenburg syndrome, domestic cat Waardenburg syndrome that occurs in domestic cat.
MONDO:1011618 Waardenburg syndrome, golden hamster Waardenburg syndrome that occurs in golden hamster.
MONDO:1011619 Wilms tumor, cattle Wilms tumour that occurs in cattle.
MONDO:1011620 Wilms tumor, dog Wilms tumour that occurs in dog.
MONDO:1011621 Wilms tumor, pig Wilms tumour that occurs in pig.
MONDO:1011622 Wilms tumor, sheep Wilms tumour that occurs in sheep.
MONDO:1011623 xanthinuria, dog Xanthinuria that occurs in dog.
MONDO:1011624 xanthinuria, domestic cat Xanthinuria that occurs in domestic cat.
MONDO:1011625 xanthinuria, goat Xanthinuria that occurs in goat.
MONDO:1011626 hyperkinesis, non-human animal
MONDO:1011627 myoclonus epilepsy of Lafora, non-human animal
MONDO:1011628 paroxysm, non-human animal
MONDO:1011629 quaking, non-human animal
MONDO:1011630 congenital lethal spasms, non-human animal
MONDO:1011631 stringhalt, non-human animal
MONDO:1011632 tetanic torticollar spasms, non-human animal
MONDO:1011633 progressive ataxia, non-human animal
MONDO:1011634 self-mutilation syndrome, non-human animal
MONDO:1011635 familial convulsions and ataxia, non-human animal
MONDO:1011636 compulsive disorder, non-human animal
MONDO:1011637 juvenile idiopathic epilepsy, non-human animal
MONDO:1011638 attention deficit hyperactivity disorder, non-human animal
MONDO:1011639 generalized myoclonic epilepsy with photosensitivity, non-human animal
MONDO:1011640 atrial septal defect and atrial fibrillation, non-human animal
MONDO:1011641 cardiomyopathy and woolly haircoat syndrome, non-human animal
MONDO:1011642 spontaneous cardiomyopathy, non-human animal
MONDO:1011643 mitral valve disease, non-human animal
MONDO:1011644 persistent right aortic arch, non-human animal
MONDO:1011645 ventricular arrhythmias and sudden death, non-human animal
MONDO:1011646 persistent truncus arteriosus with ventricular septal defect and patent foramen ovale, non-human animal
MONDO:1011647 chronic valvular disease, non-human animal
MONDO:1011648 familial thoracic aortic aneurysm, non-human animal
MONDO:1011649 persistent right aortic arch with subclavian artery and ligamentum arteriosum, non-human animal
MONDO:1011650 pentalogy of Fallot, non-human animal
MONDO:1011651 cardiomyopathy and juvenile mortality, non-human animal
MONDO:1011652 mitral valve dysplasia, non-human animal
MONDO:1011653 craniomandibular osteopathy, non-human animal
MONDO:1011654 facial digital syndrome, non-human animal
MONDO:1011655 polled and multisystemic syndrome, non-human animal
MONDO:1011656 facial dysplasia syndrome, non-human animal
MONDO:1011657 goldenhar syndrome, non-human animal
MONDO:1011658 calvarial hyperostotic syndrome, non-human animal
MONDO:1011659 gastric dilatation volvulus syndrome, non-human animal
MONDO:1011660 megaesophagus, non-human animal
MONDO:1011661 esophageal motility disorder, non-human animal
MONDO:1011662 stomach ulcer, non-human animal
MONDO:1011663 displaced abomasum, non-human animal
MONDO:1011664 gluten-sensitive enteropathy, non-human animal
MONDO:1011665 anal furunculosis, non-human animal
MONDO:1011666 non-specific digestive disorder, non-human animal
MONDO:1011667 Lundehund syndrome, non-human animal
MONDO:1011668 perosomus elumbis, non-human animal
MONDO:1011669 spina bifida with myelomeningocele, non-human animal
MONDO:1011670 spina bifida with raduschisis, non-human animal
MONDO:1011671 spinal dysraphism, non-human animal
MONDO:1011672 hydrallantois, non-human animal
MONDO:1011673 spontaneous autoimmune thyroiditis, non-human animal
MONDO:1011674 hyperosmolar nonketotic diabetes mellitus, non-human animal
MONDO:1011675 hypoadrenocorticism, non-human animal
MONDO:1011676 primary hypoadrenocorticism, non-human animal
MONDO:1011677 congenital hypoplasia of mammary gland, non-human animal
MONDO:1011678 primary hypothyroidism, non-human animal
MONDO:1011679 hereditary pancreatitis, non-human animal
MONDO:1011680 postpartum dysgalactia syndrome, non-human animal
MONDO:1011681 ACTH-independent adrenal Cushing syndrome, non-human animal
MONDO:1011682 anal gland disease, non-human animal
MONDO:1011683 caprine-like generalized hypoplasia syndrome, non-human animal
MONDO:1011684 alloimmune hemolytic anemia of the newborn, non-human animal
MONDO:1011685 bleeding disorder, non-human animal
MONDO:1011686 contact activation defect, non-human animal
MONDO:1011687 cyclic neutropenia, non-human animal
MONDO:1011688 congenital dyserythropoietic anemia with dyskeratosis and progressive alopecia, non-human animal
MONDO:1011689 hemolytic anemia, non-human animal
MONDO:1011690 primary autoimmune hemolytic anemia, non-human animal
MONDO:1011691 platelet function defect, non-human animal
MONDO:1011692 protein C deficiency, non-human animal
MONDO:1011693 reduced glutathione deficiency due to GCS deficiency, non-human animal
MONDO:1011694 thrombasthenia, non-human animal
MONDO:1011695 thrombopathia, non-human animal
MONDO:1011696 stomatocytosis and gastrits, non-human animal
MONDO:1011697 hemophagocytic syndrome, non-human animal
MONDO:1011698 reduced glutathione deficiency due to amino-acid transport defect, non-human animal
MONDO:1011699 reduced glutathione deficiency, non-human animal
MONDO:1011700 trapped neutrophil syndrome, non-human animal
MONDO:1011701 combined deficiency of factors IX and XII, non-human animal
MONDO:1011702 neonatal pancytopenia, non-human animal
MONDO:1011703 selective ADP deficiency, non-human animal
MONDO:1011704 exercise-induced pulmonary hemorrhage, non-human animal
MONDO:1011705 combined deficiency of factors VIII, IX, and X, non-human animal
MONDO:1011706 atypical thrombasthenia, non-human animal
MONDO:1011707 congenital dyserythropoietic anemia, non-human animal
MONDO:1011708 dyserythropoietic anemia and myopathy syndrome, non-human animal
MONDO:1011709 ear necrosis syndrome, non-human animal
MONDO:1011710 bilateral deafness and vestibular dysfunction, non-human animal
MONDO:1011711 unilateral deafness and vestibular dysfunction, non-human animal
MONDO:1011712 alloxan-diabetes, non-human animal
MONDO:1011713 malignant hyperthermia, non-human animal
MONDO:1011714 hypocatalasia, non-human animal
MONDO:1011715 pseudocholinesterase deficiency, non-human animal
MONDO:1011716 hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, non-human animal
MONDO:1011717 pulmonary hypoplasia with anasarca, non-human animal
MONDO:1011718 Kurosawa and Kusanagi hypercholesterolaemia, non-human animal
MONDO:1011719 intestinal cobalamin (vitamin B12) malabsorption, non-human animal
MONDO:1011720 subclinical hypocalcemia, non-human animal
MONDO:1011721 subclinical hypomagnesemia, non-human animal
MONDO:1011722 cytochrome B-related exercise intolerance, non-human animal
MONDO:1011723 mitochondrial fission encephalopathy, non-human animal
MONDO:1011724 immunodeficiency disease, non-human animal
MONDO:1011725 immunoglobulin 7S deficiency, non-human animal
MONDO:1011726 immunoglobulin A deficiency, non-human animal
MONDO:1011727 immunoglobulin G deficiency, non-human animal
MONDO:1011728 immunoglobulin G2 deficiency, non-human animal
MONDO:1011729 immunoglobulin M deficiency, non-human animal
MONDO:1011730 complement component 4 deficiency, non-human animal
MONDO:1011731 multiple autoimmune diseases syndrome, non-human animal
MONDO:1011732 autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, non-human animal
MONDO:1011733 atopy, non-human animal
MONDO:1011734 black hair follicular dysplasia, non-human animal
MONDO:1011735 dermal allergy, non-human animal
MONDO:1011736 dermatosis vegetans, non-human animal
MONDO:1011737 dystrophic epidermolysis bullosa, non-human animal
MONDO:1011738 focal metatarsal fistula, non-human animal
MONDO:1011739 congenital hypotrichosis with thymic aplasia, non-human animal
MONDO:1011740 primary seborrhea-oleosa, non-human animal
MONDO:1011741 cutaneous papillomatosis, non-human animal
MONDO:1011742 congenital erythropoietic porphyria, non-human animal
MONDO:1011743 nodular dermatofibrosis and kidney disease, non-human animal
MONDO:1011744 cutaneous and renal vasculopathy, non-human animal
MONDO:1011745 comedo syndrome, non-human animal
MONDO:1011746 facial eczema, non-human animal
MONDO:1011747 recessive hypotrichosis, non-human animal
MONDO:1011748 urticaria pigmentosa, non-human animal
MONDO:1011749 linear IgA disease, non-human animal
MONDO:1011750 follicular dysplasia and interface dermatitis, non-human animal
MONDO:1011751 acrochordonous plaque, non-human animal
MONDO:1011752 nasal parakeratosis, non-human animal
MONDO:1011753 juvenile with age-dependent emphysema hypotrichosis, non-human animal
MONDO:1011754 reactive perforating collagenosis, non-human animal
MONDO:1011755 sebaceous adenitis, non-human animal
MONDO:1011756 exfoliative cutaneous lupus erythematosus, non-human animal
MONDO:1011757 sebaceous gland dysplasia, non-human animal
MONDO:1011758 zinc deficiency-like syndrome, non-human animal
MONDO:1011759 hypotrichosis with short life expectancy, non-human animal
MONDO:1011760 symmetrical onychomadesis, non-human animal
MONDO:1011761 naked foal syndrome, non-human animal
MONDO:1011762 verrucous epidermal keratinocytic nevi, non-human animal
MONDO:1011763 lethal acrodermatitis, non-human animal
MONDO:1011764 ichthyosis fetalis, non-human animal
MONDO:1011765 micromelia, non-human animal
MONDO:1011766 warts between hooves, non-human animal
MONDO:1011767 laminitis, non-human animal
MONDO:1011768 bone spavin, non-human animal
MONDO:1011769 dysplasia epiphysealis hememelica, non-human animal
MONDO:1011770 necrosis of digits, non-human animal
MONDO:1011771 medial coronoid disease, non-human animal
MONDO:1011772 hoof wall separation syndrome, non-human animal
MONDO:1011773 degenerative suspensory ligament desmitis, non-human animal
MONDO:1011774 digital dermatitis, non-human animal
MONDO:1011775 idiopathic hepatic fibrosis, non-human animal
MONDO:1011776 inborn error of hepatic metabolism, non-human animal
MONDO:1011777 portosystemic hepatic encephalopathy, non-human animal
MONDO:1011778 chronic active hepatitis, non-human animal
MONDO:1011779 neonatal hepatitis, non-human animal
MONDO:1011780 gallbladder mucocele, non-human animal
MONDO:1011781 congential hepatic fibrosis, non-human animal
MONDO:1011782 hepatocellular fibrinogen storage disease, non-human animal
MONDO:1011783 alpha fucosidosis, non-human animal
MONDO:1011784 premature senesence, non-human animal
MONDO:1011785 lethal multi-organ developmental dysplasia, non-human animal
MONDO:1011786 perinatal weak calf syndrome, non-human animal
MONDO:1011787 degenerative myopathy of deep pectoral muscle, non-human animal
MONDO:1011788 degenerative myopathy of obturator-externus, non-human animal
MONDO:1011789 fibrodysplasia ossificans, non-human animal
MONDO:1011790 dysphagia-associated muscular dystrophy, non-human animal
MONDO:1011791 mitochondrial myopathy, non-human animal
MONDO:1011792 subacute progressive myopathy, non-human animal
MONDO:1011793 progressive myopathy, non-human animal
MONDO:1011794 spastic lameness, non-human animal
MONDO:1011795 masticatory muscle myositis, non-human animal
MONDO:1011796 high-frequency tremor, non-human animal
MONDO:1011797 myopathy of the diaphragmatic muscles, non-human animal
MONDO:1011798 forelimb-girdle muscular anomaly, non-human animal
MONDO:1011799 inherited periodic spasticity, non-human animal
MONDO:1011800 contractural arachnodactyly, non-human animal
MONDO:1011801 type 2 polysaccharide storage myopathy, non-human animal
MONDO:1011802 congenital merosin-deficient muscular dystrophy, non-human animal
MONDO:1011803 muscular dystrophy-dystroglycanopathy (limb-girdle), non-human animal
MONDO:1011804 congenital myopathy with fiber-type disproportion, non-human animal
MONDO:1011805 exercise induced metabolic myopathy, non-human animal
MONDO:1011806 immune-mediated myositis, non-human animal
MONDO:1011807 atypical myopathy, non-human animal
MONDO:1011808 Hodgkin disease, non-human animal
MONDO:1011809 multiple lipomatosis, non-human animal
MONDO:1011810 megakaryoblastic leukemia, non-human animal
MONDO:1011811 congenital melanoma, non-human animal
MONDO:1011812 ocular squamous cell carcinoma, non-human animal
MONDO:1011813 sarcoid, non-human animal
MONDO:1011814 melanoblastoma, non-human animal
MONDO:1011815 renal cystadenocarcinoma and nodular dermatofibrosis, non-human animal
MONDO:1011816 lymphoproliferative disease, non-human animal
MONDO:1011817 anal sac gland carcinoma, non-human animal
MONDO:1011818 invasive transitional cell carcinoma, non-human animal
MONDO:1011819 chronic myelogenous leukemia, non-human animal
MONDO:1011820 colorectal hamartomatous polyposis and ganglioneuromatosis, non-human animal
MONDO:1011821 malignant melanoma, non-human animal
MONDO:1011822 squamous cell carcinoma of the digit, non-human animal
MONDO:1011823 hemangiosarcoma, non-human animal
MONDO:1011824 horn cancer, non-human animal
MONDO:1011825 choroid plexus tumour, non-human animal
MONDO:1011826 dysplastic gangliocytoma of the cerebellum, non-human animal
MONDO:1011827 congenital mast cell tumor, non-human animal
MONDO:1011828 cancer, non-human animal
MONDO:1011829 progressive ataxia with degenerative thoracic myelopathy, non-human animal
MONDO:1011830 audiogenic seizure, non-human animal
MONDO:1011831 distal axonopathy, non-human animal
MONDO:1011832 peripheral axonopathy, non-human animal
MONDO:1011833 cerebellar Purkinje cell degeneration, non-human animal
MONDO:1011834 cerebellar abiotrophy, non-human animal
MONDO:1011835 congenital cerebellar anomaly, non-human animal
MONDO:1011836 cerebellar cortical atrophy, non-human animal
MONDO:1011837 cerebellar disease, non-human animal
MONDO:1011838 congenital copper deficiency, non-human animal
MONDO:1011839 degenerative myelopathy, non-human animal
MONDO:1011840 delta 9-tetrahydrocannabinol seizure, non-human animal
MONDO:1011841 faded shaker, non-human animal
MONDO:1011842 granule cell type cerebellar hypoplasia, non-human animal
MONDO:1011843 internal hydrocephalus, non-human animal
MONDO:1011844 hypertrophic neuropathy, non-human animal
MONDO:1011845 congenital hypomyelinogenesis, non-human animal
MONDO:1011846 hypothalamic dysplasia, non-human animal
MONDO:1011847 hypotrophic axonopathy, non-human animal
MONDO:1011848 lower motor neuron disease, non-human animal
MONDO:1011849 myasthenia, non-human animal
MONDO:1011850 necrotising myelopathy, non-human animal
MONDO:1011851 congenital neuromuscular disease, non-human animal
MONDO:1011852 neurogenic muscular atrophy, non-human animal
MONDO:1011853 neurological syndrome, non-human animal
MONDO:1011854 thalamic-cerebellar neuropathy, non-human animal
MONDO:1011855 distal sensorimotor polyneuropathy, non-human animal
MONDO:1011856 progressive axonopathy, non-human animal
MONDO:1011857 progressive cerebellar abiotrophy, non-human animal
MONDO:1011858 progressive spinal myelopathy, non-human animal
MONDO:1011859 spastic paresis, non-human animal
MONDO:1011860 spastic syndrome, non-human animal
MONDO:1011861 tremor, non-human animal
MONDO:1011862 tremor syndrome with central axonopathy, non-human animal
MONDO:1011863 subacute necrotising encephalopathy of Leigh, non-human animal
MONDO:1011864 polymicrogyria and asymmetrical ventricular dilation, non-human animal
MONDO:1011865 axonopathy, non-human animal
MONDO:1011866 degenerative myeloencephalopathy, non-human animal
MONDO:1011867 neuronal abiotrophy, non-human animal
MONDO:1011868 motor neuron disease, non-human animal
MONDO:1011869 spinal dysmyelination, non-human animal
MONDO:1011870 polioencephalomyelopathy, non-human animal
MONDO:1011871 progressive neuronopathy, non-human animal
MONDO:1011872 polyneuropathy, non-human animal
MONDO:1011873 neuronal vacuolar disorder, non-human animal
MONDO:1011874 degenerative neuromuscular disease, non-human animal
MONDO:1011875 progressive ataxia with head tremor and seizures, non-human animal
MONDO:1011876 unilateral subcortical heterotopia, non-human animal
MONDO:1011877 exercise-induced collapse, non-human animal
MONDO:1011878 sensory ataxic neuropathy, non-human animal
MONDO:1011879 necrotizing meningoencephalitis, non-human animal
MONDO:1011880 neonatal encephalopathy with seizures, non-human animal
MONDO:1011881 tomaculous neuropathy, non-human animal
MONDO:1011882 segmental axonopathy, non-human animal
MONDO:1011883 dilute coat color with neurological defects, non-human animal
MONDO:1011884 acral mutilation syndrome, non-human animal
MONDO:1011885 episodic falling, non-human animal
MONDO:1011886 neuroaxonal dystrophy with cerebellar abiotrophy, non-human animal
MONDO:1011887 retinal dysplasia and internal hydrocephalus, non-human animal
MONDO:1011888 congenital hydranencephaly and cerebellar hypoplasia, non-human animal
MONDO:1011889 familial episodic spinocerebellar ataxia, non-human animal
MONDO:1011890 leukoencephalomyelopathy, non-human animal
MONDO:1011891 cervical vertebral compressive myelopathy, non-human animal
MONDO:1011892 spinal intradural arachnoid cyst, non-human animal
MONDO:1011893 neurodegenerative vacuolar storage disease, non-human animal
MONDO:1011894 degenerative encephalopathy, non-human animal
MONDO:1011895 Guillain-Barr-like polyradiculoneuropathy, non-human animal
MONDO:1011897 cavitating leukodystrophy, non-human animal
MONDO:1011898 hypomyelinating leukodystrophy, non-human animal
MONDO:1011899 olivopontocerebellar degeneration, non-human animal
MONDO:1011900 hypopigmentation and deafness, non-human animal
MONDO:1011901 white skin color and iridophoroma, non-human animal
MONDO:1011902 neuropathy and feather color dilution, non-human animal
MONDO:1011903 renal amyloidosis, non-human animal
MONDO:1011904 chronic interstitial nephropathy, non-human animal
MONDO:1011905 glomerulonephropathy, non-human animal
MONDO:1011906 hemolytic uremic syndrome, non-human animal
MONDO:1011907 nephropathy, non-human animal
MONDO:1011908 polycystic mononephrosis, non-human animal
MONDO:1011909 renal disease, non-human animal
MONDO:1011910 renal dysplasia and bladder aplasia-hypoplasia, non-human animal
MONDO:1011911 renal insufficiency, non-human animal
MONDO:1011912 renal nephropathy, non-human animal
MONDO:1011913 renal cysts, non-human animal
MONDO:1011914 protein-losing nephropathy, non-human animal
MONDO:1011915 diffuse cystic renal dysplasia and hepatic fibrosis, non-human animal
MONDO:1011916 Meckel-like hepatorenal fibrocystic dysplasia syndrome, non-human animal
MONDO:1011917 idiopathic hypercalciuria, non-human animal
MONDO:1011918 tetragametic chimerism, non-human animal
MONDO:1011919 androgen insensitivity syndrome, non-human animal
MONDO:1011920 yellow-semen syndrome, non-human animal
MONDO:1011921 pyometra, non-human animal
MONDO:1011922 retained placenta, non-human animal
MONDO:1011923 respiratory distress syndrome, non-human animal
MONDO:1011924 brachycephalic airway obstruction syndrome, non-human animal
MONDO:1011925 primary ciliary dyskinesia, non-human animal
MONDO:1011926 shivers, non-human animal
MONDO:1011927 pulmonary adenomatosis, non-human animal
MONDO:1011928 laryngeal paralysis, generic, non-human animal
MONDO:1011929 guttural pouch tympany, non-human animal
MONDO:1011930 recurrent airway obstruction, non-human animal
MONDO:1011931 upper airway syndrome, non-human animal
MONDO:1011932 recurrent inflammatory pulmonary disease, non-human animal
MONDO:1011933 pulmonary surfactant metabolism dysfunction, non-human animal
MONDO:1011934 laryngeal collapse, dynamic, non-human animal
MONDO:1011935 growth and respiratory lethal syndrome, non-human animal
MONDO:1011936 arthritis deformans, non-human animal
MONDO:1011937 type-II collagen-immune complex arthritis, non-human animal
MONDO:1011938 arthrogryposis and palatoschisis syndrome, non-human animal
MONDO:1011939 brachygnathia superior and degenerative joint disease, non-human animal
MONDO:1011940 ocular-skeletal dysplasia, non-human animal
MONDO:1011941 Ancon dwarfism, non-human animal
MONDO:1011942 autosomal dwarfism, non-human animal
MONDO:1011943 pituitary dwarfism, non-human animal
MONDO:1011944 multiple exostoses, non-human animal
MONDO:1011945 hypothyroidism and dwarfism, non-human animal
MONDO:1011946 congenital joint laxity and dwarfism, non-human animal
MONDO:1011947 muscle contracture and chondrodysplasia, non-human animal
MONDO:1011948 navicular disease, non-human animal
MONDO:1011949 occipital dysplasia, non-human animal
MONDO:1011950 osteochondroma causing progressive posterior paresis, non-human animal
MONDO:1011951 osteodystrophy, non-human animal
MONDO:1011952 polyarthritis, non-human animal
MONDO:1011953 spinal dysplasia, non-human animal
MONDO:1011954 tibial dyschondroplasia, non-human animal
MONDO:1011955 spondylosis deformans, non-human animal
MONDO:1011956 growth-hormone-receptor deficiency dwarfism, non-human animal
MONDO:1011957 hypochondroplastic dwarfism, non-human animal
MONDO:1011958 Laron dwarfism, non-human animal
MONDO:1011959 growth-hormone deficiency dwarfism,, non-human animal
MONDO:1011960 rupture of the cranial cruciate ligament, non-human animal
MONDO:1011961 brachygnathia, cardiomegaly and renal hypoplasia syndrome, non-human animal
MONDO:1011962 vitamin D-deficiency rickets, non-type I, non-type II, non-human animal
MONDO:1011963 proportionate dwarfism with inflammatory lesions, non-human animal
MONDO:1011964 idiopathic congenital chondrodystrophy, non-human animal
MONDO:1011965 disproportionate short-limbed chondrodysplasia, non-human animal
MONDO:1011966 skeletal dysplasia with craniofacial deformity and disproportionate dwarfism, non-human animal
MONDO:1011967 vertebral and spinal dysplasia, non-human animal
MONDO:1011968 lethal arthrogryposis syndrome, non-human animal
MONDO:1011969 Dahlem dwarfism, non-human animal
MONDO:1011970 asymmetrical occipital condylar dysplasia, non-human animal
MONDO:1011971 caudal cruciate ligament disease, non-human animal
MONDO:1011972 osteochondromatosis, non-human animal
MONDO:1011973 pyknodysostosis, non-human animal
MONDO:1011974 aniridia with cataract, non-human animal
MONDO:1011975 congenital blindness, non-human animal
MONDO:1011976 Collie eye anomaly, non-human animal
MONDO:1011977 progressive retinal atrophy, non-human animal
MONDO:1011978 central retinal degeneration, non-human animal
MONDO:1011979 retinal dysplasia, non-human animal
MONDO:1011980 retinal dystrophy, non-human animal
MONDO:1011981 rod-cone degeneration, non-human animal
MONDO:1011982 rod-cone dysplasia, non-human animal
MONDO:1011983 tapetal degeneration, non-human animal
MONDO:1011984 retinal and skeletal dysplasia, non-human animal
MONDO:1011985 early retinal degeneration, non-human animal
MONDO:1011986 progressive rod-cone degeneration, non-human animal
MONDO:1011987 photoreceptor dysplasia, non-human animal
MONDO:1011988 retinal dysplasia and degeneration, non-human animal
MONDO:1011989 blindness with enlarged globe, non-human animal
MONDO:1011990 retinal dysplasia and persistent primary vitreous, non-human animal
MONDO:1011991 rod dysplasia, non-human animal
MONDO:1011992 congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, non-human animal
MONDO:1011993 lacrimal fistula, non-human animal
MONDO:1011994 fluoroquinolone-induced retinal degeneration, non-human animal
MONDO:1011995 gyrate atrophy of choroid and retina, non-human animal
MONDO:1011996 ocular melanosis, non-human animal
MONDO:1011997 recurrent uveitis, non-human animal
MONDO:1011998 primary open angle glaucoma, non-human animal
MONDO:1011999 pectinate ligament dysplasia, non-human animal
MONDO:1012000 sudden acquired retinal degeneration syndrome, non-human animal
MONDO:1012001 bilateral corneal stromal loss, non-human animal
MONDO:1012002 vitreous degeneration, non-human animal
MONDO:1012003 corneal sequestra, non-human animal
MONDO:1012004 osseous choristoma of the ciliary body, non-human animal
MONDO:1030002 dysplasia of the proximal femoral epiphyses A developmental disorder affecting the growth and development of the proximal end of the femur (thigh bone) near the hip joint characterized by avascular necrosis of the femoral head, cystic changes of the femoral head, and/or sclerosis of the femoral head. It is a relatively milder form of the other skeletal disorders associated with COL2A1.

Changed terms

Changed labels

Mondo ID Label Previous release New release
MONDO:0013881 epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome pidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
MONDO:0014347 Rothmund-Thomson syndrome, type 3 short stature with microcephaly and distinctive facies Rothmund-Thomson syndrome, type 3

Changed definitions

Mondo ID Label Previous release New release
MONDO:0100016 early-onset generalized dystonia A generalized isolated dystonia characterized by early-onset, which may be clinically indistinguishable from DYT-TOR1A and may be the most common cause of early-onset generalized dystonia, at least outside the Askenazi Jewish population.
MONDO:0859050 Schistosoma mansoni infection, susceptibility/resistance to An inherited predisposition to Schistosoma mansoni infection intensity and reinfection after treatment.
MONDO:0060778 adult Fanconi syndrome Probably related to a recessive gene, this is Fanconi Syndrome, characterized by adult onset. A Fanconi renotubular syndrome that occurs in an adult. Adult Fanconi syndrome is typically acquired.

Obsolete terms

Mondo ID Label
MONDO:0000093 obsolete Schistosoma mansoni infection, susceptibility
MONDO:0002839 obsolete leather-bottle stomach
MONDO:0006788 obsolete hydrophthalmos
MONDO:0009586 obsolete mesangial sclerosis, diffuse renal, with ocular abnormalities
MONDO:0100032 obsolete familial temporal lobe epilepsy syndrome

New obsoletion candidates

Mondo ID Label
MONDO:0000014 colorblindness, partial
MONDO:0000114 cerebelloparenchymal disorder
MONDO:0018234 dysostosis
MONDO:0000224 acquired carbohydrate metabolism disease
MONDO:0000251 diarrheal disease secondary to altered bowel motility
MONDO:0037938 inborn disorder of aspartate family metabolism
MONDO:0000379 malignant Sertoli-Leydig cell tumor
MONDO:0021635 neurocristopathy
MONDO:0024479 epithelial tumor of colon
MONDO:0024476 epithelial neoplasm of rectum
MONDO:0020672 vascular occlusion disorder
MONDO:0001394 chronic erythremia
MONDO:0045004 skeletal ligament disorder
MONDO:0021260 sensory ganglionopathy
MONDO:0005179 ovarian adenoma benign
MONDO:0004603 collagenopathy
MONDO:0004961 stage I endometrioid carcinoma
MONDO:0004962 stage II endometrioid carcinoma
MONDO:0005168 neoplasm of immature B and T cells
MONDO:0100030 adolescent/adult-onset epilepsy syndrome
MONDO:0005254 symptomatic heart failure
MONDO:0005255 mild heart failure
MONDO:0005256 moderate heart failure
MONDO:0005257 advanced heart failure
MONDO:0005426 MRI defined brain infarct
MONDO:0005430 early onset hypertension
MONDO:0005432 alcohol and nicotine codependence
MONDO:0005435 anti-neutrophil antibody associated vasculitis
MONDO:0005436 postoperative ventricular dysfunction
MONDO:0005465 methamphetamine-induced psychosis
MONDO:0005470 postprandial hypotension
MONDO:0005471 neurally mediated hypotension
MONDO:0005493 carbon monoxide-induced delayed encephalopathy
MONDO:0005585 chemotherapy-induced hypertension
MONDO:0005597 cystic renal cell carcinoma
MONDO:0005598 dopaminergic neuroblastoma
MONDO:0006027 breast synovial sarcoma
MONDO:0042973 familial osteosclerosis
MONDO:0007466 DNA, satellite, 3
MONDO:0016420 familial flecked retinopathy
MONDO:0015083 nuclear oculomotor paralysis
MONDO:0020173 benign tumor of palpebral epidermis
MONDO:0016697 low grade ependymoma
MONDO:0100029 antibody mediated epilepsy
MONDO:0009455 immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes
MONDO:0100080 cardioectodermal syndrome
MONDO:0011292 dermatitis, atopic
MONDO:0023224 inherited reflex epilepsy
MONDO:0015174 autoimmune enteropathy type 3
MONDO:0022606 branchial arch disease
MONDO:0015256 blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome
MONDO:0015257 sino-auricular heart block
MONDO:0024322 disorder of glycosylation
MONDO:0015424 lethal chondrodysplasia, Moerman type
MONDO:0015468 craniosynostosis-cataract syndrome
MONDO:0015559 lymphoadenopathic mastocytosis with eosinophilia
MONDO:0015907 epimetaphyseal skeletal dysplasia
MONDO:0015985 bone dysplasia, Azouz type
MONDO:0100022 neonatal/infantile epilepsy syndrome
MONDO:0016271 adenoid cystic carcinoma of the corpus uteri
MONDO:0016583 familial intestinal malrotation-facial anomalies syndrome
MONDO:0016821 shoulder and girdle defects-familial intellectual disability syndrome
MONDO:0016827 myopathy-growth delay-intellectual disability-hypospadias syndrome
MONDO:0016857 blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome
MONDO:0016858 blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome
MONDO:0016859 blepharophimosis-epicanthus inversus-ptosis due to copy number variations
MONDO:0017047 infantile axonal neuropathy
MONDO:0017126 oculo-skeletal-renal syndrome
MONDO:0017451 non-syndromic brachydactyly of fingers
MONDO:0017472 patella aplasia/hypoplasia, unilateral
MONDO:0017473 patella aplasia/hypoplasia, bilateral
MONDO:0017478 amelia of upper limb, unilateral
MONDO:0017479 amelia of upper limb, bilateral
MONDO:0017480 amelia of lower limb, unilateral
MONDO:0017482 humeral agenesis/hypoplasia, unilateral
MONDO:0017483 humeral agenesis/hypoplasia, bilateral
MONDO:0017484 femoral agenesis/hypoplasia, unilateral
MONDO:0017485 femoral agenesis/hypoplasia, bilateral
MONDO:0017486 radial hemimelia, unilateral
MONDO:0017487 radial hemimelia, bilateral
MONDO:0017488 ulnar hemimelia, bilateral
MONDO:0017489 ulnar hemimelia, unilateral
MONDO:0017490 tibial hemimelia, unilateral
MONDO:0017492 fibular hemimelia, unilateral
MONDO:0017493 fibular hemimelia, bilateral
MONDO:0017496 congenital absence of thigh and lower leg with foot present, unilateral
MONDO:0017498 congenital absence of both forearm and hand, unilateral
MONDO:0017500 congenital absence of both lower leg and foot, unilateral
MONDO:0017502 acheiria, unilateral
MONDO:0017504 apodia, unilateral
MONDO:0017509 adactyly of foot, unilateral
MONDO:0017511 split hand, unilateral
MONDO:0017513 split foot, unilateral
MONDO:0017515 brachydactyly of fingers, unilateral
MONDO:0017517 brachydactyly of toes, unilateral
MONDO:0017519 symbrachydactyly of hand and foot, unilateral
MONDO:0017521 hyperphalangy, unilateral
MONDO:0017522 hyperphalangy, bilateral
MONDO:0017523 polydactyly of a biphalangeal thumb, unilateral
MONDO:0017524 polydactyly of a biphalangeal thumb, bilateral
MONDO:0017525 polydactyly of a triphalangeal thumb, unilateral
MONDO:0017526 polydactyly of a triphalangeal thumb, bilateral
MONDO:0017527 polydactyly of an index finger, unilateral
MONDO:0017529 polysyndactyly, unilateral
MONDO:0017530 polysyndactyly, bilateral
MONDO:0017531 postaxial polydactyly type A, unilateral
MONDO:0017532 postaxial polydactyly type A, bilateral
MONDO:0017533 postaxial polydactyly type B, unilateral
MONDO:0017534 postaxial polydactyly type B, bilateral
MONDO:0017535 central polydactyly of fingers, unilateral
MONDO:0017537 Preaxial polydactyly of toes, unilateral
MONDO:0017548 humero-radio-ulnar synostosis, unilateral
MONDO:0017550 humero-radial synostosis, unilateral
MONDO:0017551 humero-radial synostosis, bilateral
MONDO:0017556 Madelung deformity, unilateral
MONDO:0017562 congenital patella dislocation, unilateral
MONDO:0017613 intellectual disability-hypotonia-skin hyperpigmentation syndrome
MONDO:0017616 X-linked intellectual disability, Schutz type
MONDO:0017642 intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome
MONDO:0024321 disorder of GPI anchor biosynthesis
MONDO:0018503 carcinoma of stomach, salivary gland type
MONDO:0019397 unknown leukodystrophy
MONDO:0019417 X-linked intellectual disability-precocious puberty-obesity syndrome
MONDO:0019649 idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis
MONDO:0019650 idiopathic steroid-sensitive nephrotic syndrome with minimal change
MONDO:0019651 idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation
MONDO:0019652 familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
MONDO:0019653 familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
MONDO:0019654 familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
MONDO:0019655 sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
MONDO:0019656 sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
MONDO:0019738 atypical hemolytic-uremic syndrome with H factor anomaly
MONDO:0019752 pediatric Castleman disease
MONDO:0019770 X-linked dominant intellectual disability-epilepsy syndrome
MONDO:0019821 aneurysm or dilatation of ascending aorta
MONDO:0019986 sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy
MONDO:0021017 synaptopathy
MONDO:0020183 neurogenic palpebral tumor
MONDO:0020252 essential strabismus
MONDO:0020353 von Hippel anomaly
MONDO:0020477 progeria-associated arthropathy
MONDO:0020637 Mendelian susceptibility to mycobacterial diseases due to a partial deficiency
MONDO:0020651 mixed germ cell tumor of vulva
MONDO:0020652 immature teratoma of vulva
MONDO:0021130 disorder of sphingolipid biosynthesis
MONDO:0021762 acrocoxomesomelic dysplasia
MONDO:0021764 acrofacial dysostosis Preis type
MONDO:0021905 Apert-like polydactyly syndrome
MONDO:0021907 aplasia cutis autosomal recessive
MONDO:0021908 aplasia cutis congenita dominant
MONDO:0022380 acute lymphoblastic leukemia congenital sporadic aniridia
MONDO:0022398 aglossia and situs inversus
MONDO:0022401 agyria pachygyria polymicrogyria
MONDO:0022402 agyria-pachygyria type 1
MONDO:0022413 Albright-like syndrome
MONDO:0022444 amyloidosis bronchopulmonary
MONDO:0022454 angiosarcoma of the scalp
MONDO:0022456 ankle defects short stature
MONDO:0022457 ankyloblepharon filiforme imperforate anus
MONDO:0022458 annular constricting bands
MONDO:0022461 anophthalmia cleft palate micrognathia
MONDO:0022462 anophthalmia esophageal atresia cryptorchidism
MONDO:0022465 anotia facial palsy cardiac defect
MONDO:0022470 aortic dissection lentiginosis
MONDO:0022471 childhood aortic valve stenosis
MONDO:0022481 APO A-i deficiency
MONDO:0022500 arthrogryposis multiplex congenita CNS calcification
MONDO:0022504 arthrogryposis spinal muscular atrophy
MONDO:0022553 BD syndrome
MONDO:0022572 bilateral renal agenesis dominant type
MONDO:0022573 biliary atresia intrahepatic non syndromic form
MONDO:0022574 biliary atresia intrahepatic syndromic form
MONDO:0022576 bilirubin induced brain injury in the newborn
MONDO:0022580 blepharo naso facial syndrome van Maldergem type
MONDO:0022586 bone dysplasia Moore type
MONDO:0022587 bone dysplasia corpus callosum agenesis
MONDO:0022598 brachydactyly absence of distal phalanges
MONDO:0022599 brachydactyly anonychia
MONDO:0022602 brachydactyly small stature face anomalies
MONDO:0022603 brachydactyly tibial hypoplasia
MONDO:0022608 brittle bone syndrome lethal type
MONDO:0022610 bronchiectasis oligospermia
MONDO:0022613 bruyn scheltens syndrome
MONDO:0022615 burn goodship syndrome
MONDO:0022622 congenital disorder of glycosylation syndrome type 4
MONDO:0022623 CDK4 linked melanoma
MONDO:0022639 Cantu Sanchez-Corona Garcia-Cruz syndrome
MONDO:0022645 cardioencephalomyopathy
MONDO:0022646 cardiofacial syndrome short limbs
MONDO:0022647 cardiomelic syndrome stratton Koehler type
MONDO:0022650 cardiomyopathy diabetes deafness
MONDO:0022655 cardiomyopathy hypogonadism metabolic anomalies
MONDO:0022656 cardiomyopathy spherocytosis
MONDO:0022662 carpo tarsal osteolysis recessive
MONDO:0022675 cataract skeletal anomalies
MONDO:0022691 cerebello-olivary atrophy
MONDO:0022693 cerebral calcification cerebellar hypoplasia
MONDO:0022694 cerebral calcifications opalescent teeth phosphaturia
MONDO:0022729 chondrodysplasia punctata with steroid sulfatase deficiency
MONDO:0022733 choreoacanthocytosis amyotrophic
MONDO:0022739 Christian Demyer Franken syndrome
MONDO:0022740 Christian Johnson angenieta syndrome
MONDO:0022765 chronic demyelinizing neuropathy with IgM monoclonal
MONDO:0022768 chronic polyradiculoneuritis
MONDO:0022769 ciliary dyskinesia-bronchiectasis
MONDO:0022770 circumscribed cutaneous aplasia of the vertex
MONDO:0022771 circumscribed disseminated keratosis Jadassohn lew type
MONDO:0022775 cleft lip and palate malrotation cardiopathy
MONDO:0022776 cleft lip and/or palate with mucous cysts of lower
MONDO:0022777 cleft lip palate dysmorphism kumar type
MONDO:0022778 cleft lip palate intellectual disability corneal opacity
MONDO:0022779 cleft lip palate oligodontia syndactyly pili torti
MONDO:0022780 cleft lip palate pituitary deficiency
MONDO:0022781 cleft lip palate-tetraphocomelia
MONDO:0022782 cleft lower lip cleft lateral canthi chorioretinal
MONDO:0022785 cleft palate cardiac defect ectrodactyly
MONDO:0022786 cleft palate colobomata radial synostosis deafness
MONDO:0022787 cleft palate heart disease polydactyly absent tibia
MONDO:0022791 coarse face hypotonia constipation
MONDO:0022795 deficiency of coenzyme q cytochrome c reductase
MONDO:0022798 Cohen Lockood Wyborney syndrome
MONDO:0022802 Collins-Sakati syndrome
MONDO:0022803 coloboma porencephaly hydronephrosis
MONDO:0022804 colobomata unilobar lung heart defect
MONDO:0022809 Colver Steer Godman syndrome
MONDO:0022810 Combarros Calleja Leno syndrome
MONDO:0022818 congenital aneurysms of the great vessels
MONDO:0022821 congenital benign spinal muscular atrophy dominant
MONDO:0022824 congenital craniosynostosis maternal hyperthyroiditis
MONDO:0022826 congenital cystic eye multiple ocular and intracranial anomalies
MONDO:0022831 congenital heart disease ptosis hypodontia craniostosis
MONDO:0022832 congenital heart disease radio ulnar synostosis intellectual disability
MONDO:0022841 congenital hypotrichosis milia
MONDO:0022849 congenital stenosis of cervical medullary canal
MONDO:0022854 congenital unilateral pulmonary hypoplasia
MONDO:0022855 congenital vagal hyperreflexivity
MONDO:0022862 Cormier Rustin Munnich syndrome
MONDO:0022863 corneal crystals myopathy neuropathy
MONDO:0022865 corneal dystrophy ichthyosis microcephaly intellectual disability
MONDO:0022866 corneal dystrophy pigmentary anomaly malabsorption
MONDO:0022871 corpus callosum agenesis of blepharophimosis robin type
MONDO:0022872 corpus callosum dysgenesis X-linked recessive
MONDO:0022873 corpus callosum dysgenesis cleft spasm
MONDO:0022874 corpus callosum dysgenesis hypopituitarism
MONDO:0022875 cortada Koussef Matsumoto syndrome
MONDO:0022876 Cortes Lacassie syndrome
MONDO:0022883 craniofacial and skeletal defects
MONDO:0022887 craniofrontonasal syndrome Teebi type
MONDO:0022888 craniostenosis cataract
MONDO:0022889 craniostenosis with congenital heart disease intellectual disability
MONDO:0022890 craniosynostosis Fontaine type
MONDO:0022891 craniosynostosis Maroteaux Fonfria type
MONDO:0022892 craniosynostosis alopecia brain defect
MONDO:0022893 craniosynostosis arthrogryposis cleft palate
MONDO:0022894 craniosynostosis autosomal dominant
MONDO:0022895 craniosynostosis cleft lip palate arthrogryposis
MONDO:0022897 craniosynostosis exostoses nevus epibulbar dermoid
MONDO:0022898 craniosynostosis intellectual disability heart defects
MONDO:0022899 crawfurd syndrome
MONDO:0022907 cutaneous sclerosis
MONDO:0022908 cutis gyratum acanthosis nigricans craniosynostosis
MONDO:0022909 cutis laxa osteoporosis
MONDO:0022912 cutis verticis gyrata mental deficiency
MONDO:0022919 cytokine receptor deficiency
MONDO:0022937 deafness conductive stapedial ear malformation facial palsy
MONDO:0022938 deafness goiter stippled epiphyses
MONDO:0022941 deafness hypospadias metacarpal and metatarsal syndrome
MONDO:0022942 deafness mesenteric diverticula of small bowel neuropathy
MONDO:0022945 deafness peripheral neuropathy arterial disease
MONDO:0022946 deafness progressive cataract autosomal dominant
MONDO:0022949 defective apolipoprotein b-100
MONDO:0022960 dermatocardioskeletal syndrome boronne type
MONDO:0022971 diabetes persistent mullerian ducts
MONDO:0022975 diaphragmatic agenesis radial aplasia omphalocele
MONDO:0022977 diaphragmatic hernia exomphalos corpus callosum agenesis
MONDO:0022978 diaphragmatic hernia upper limb defects
MONDO:0022981 die Smulders droog van dijk syndrome
MONDO:0022985 diffuse cavernous hemangioma of the rectum
MONDO:0022989 diomedi bernardi placidi syndrome
MONDO:0022990 diphallus rachischisis imperforate anus
MONDO:0022999 distichiasis heart congenital anomalies
MONDO:0023003 double fingernail of fifth finger
MONDO:0023006 doxorubicin induced cardiomyopathy
MONDO:0023015 duodenal atresia tetralogy of fallot
MONDO:0023016 duplication of leg mirror foot
MONDO:0023017 duplication of the thumb unilateral biphalangeal
MONDO:0023018 dupont sellier chochillon syndrome
MONDO:0023019 dwarfism bluish sclerae
MONDO:0023020 dwarfism deafness retinitis pigmentosa
MONDO:0023021 dwarfism lethal type advanced bone age
MONDO:0023030 dysmorphism cleft palate loose skin
MONDO:0023040 ectodermal dysplasia Bartalos type
MONDO:0023042 ectodermal dysplasia margarita type
MONDO:0023045 ectodermal dysplasia arthrogryposis diabetes mellitus
MONDO:0023046 ectodermal dysplasia blindness
MONDO:0023048 ectodermal dysplasia neurosensory deafness
MONDO:0023061 enamel hypoplasia cataract hydrocephaly
MONDO:0023062 encephalocele anencephaly
MONDO:0023068 Engelhard Yatziv syndrome
MONDO:0023079 epidermal nevus vitamin D resistant rickets
MONDO:0023083 epimetaphyseal dysplasia cataract
MONDO:0023084 epiphyseal dysplasia dysmorphism camptodactyly
MONDO:0023091 esophageal atresia coloboma talipes
MONDO:0023099 FRAXD syndrome
MONDO:0023100 facial clefting corpus callosum agenesis
MONDO:0023101 facio digito genital syndrome recessive form
MONDO:0023137 feigenbaum Bergeron syndrome
MONDO:0023142 fetal brain disruption sequence
MONDO:0023148 fetal phenothiazine syndrome
MONDO:0023155 fibula aplasia complex brachydactyly
MONDO:0023157 fibular hypoplasia scapulo pelvic dysplasia absent
MONDO:0023167 focal alopecia congenital megalencephaly
MONDO:0023170 focal or multifocal malformations in neuronal migration
MONDO:0023175 Fontaine farriaux blanckaert syndrome
MONDO:0023178 fragile X syndrome type 1
MONDO:0023179 fragile X syndrome type 2
MONDO:0023180 fragile X syndrome type 3
MONDO:0023196 frontonasal malformation cloacal exstrophy
MONDO:0023197 frontonasal dysplasia Klippel feil syndrome
MONDO:0023199 frontonasal dysplasia phocomelic upper limbs
MONDO:0023200 Fryns Fabry Remans syndrome
MONDO:0023208 Fuqua Berkovitz syndrome
MONDO:0023221 Gaucher ichthyosis restrictive dermopathy
MONDO:0023226 gershinibaruch Leibo syndrome
MONDO:0023240 gigantism advanced bone age hoarse cry
MONDO:0023250 global disaccharide intolerance
MONDO:0023255 glossopalatine ankylosis micrognathia ear anomalies
MONDO:0023272 goniodysgenesis intellectual disability short stature
MONDO:0024171 radio-digito-facial dysplasia
MONDO:0024418 muscular fibrosis multifocal obstructed vessels
MONDO:0025512 type II hypersensitivity reaction disease
MONDO:0035117 PUM1-associated developmental disability-ataxia-seizure syndrome
MONDO:0035433 calpain-3-related limb-girdle muscular dystrophy D4
MONDO:0035454 B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
MONDO:0035474 PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis
MONDO:0040872 non-psychogenic polydipsia
MONDO:0043108 infantile striato thalamic degeneration
MONDO:0044763 diarrheal disease secondary to decreased bowel motility
MONDO:0044880 cystic tumor of the pancreas
MONDO:0100012 paratenonitis
MONDO:0100013 paratenonitis with tendinosis
MONDO:0100015 adult-onset segmental dystonia
MONDO:0100019 ECHS1-related paroxysmal dyskinesia
MONDO:0100020 atypical childhood epilepsy with centrotemporal spikes
MONDO:0100021 photosensitive occipital lobe epilepsy
MONDO:0100026 myoclonic encephalopathy in non-progressive disorder
MONDO:0100052 acetazolamide-responsive hereditary episodic ataxia
MONDO:0100066 TH-deficient progressive infantile encephalopathy
MONDO:0100068 SLC10A7-congenital disorder of glycosylation
MONDO:0100107 non-neonatal early infantile epileptic encephalopathy
MONDO:0100112 acyl-CoA binding domain containing protein 5 deficiency
MONDO:0100113 hearing loss with skin disease

Terms that were previously candidate for obsoletion and are now not anymore

No changes.

Assets 33
Loading