v2024-07-02

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.