Reverse bridge / human → dog
Canine natural models of human disease.
The dog is one of medicine's most powerful natural models: it shares our homes, our environment, and much of our genome, and it develops many of the same diseases spontaneously. This is the reverse of the usual bridge. Start from a human disease and see which dogs carry a natural model of it, mapped gene by gene across the ortholog bridge, ranked by evidence, and cited.
344 human diseases mapped 262 with an OMIA-anchored model
- congenital factor XI deficiency 2 OMIA 2 paths
- Duchenne muscular dystrophy 2 OMIA 2 paths
- hemophilia A 2 OMIA 2 paths
- hemophilia B 2 OMIA 2 paths
- inherited prekallikrein deficiency 2 OMIA 2 paths
- Krabbe disease 2 OMIA 2 paths
- L-2-hydroxyglutaric aciduria 2 OMIA 2 paths
- MONDO:0009710 2 OMIA 2 paths
- MONDO:0019642 2 OMIA 2 paths
- mucopolysaccharidosis type 7 2 OMIA 2 paths
- neuronal ceroid lipofuscinosis 7 2 OMIA 2 paths
- persistent Mullerian duct syndrome 2 OMIA 2 paths
- polycystic kidney disease 1 2 OMIA 2 paths
- pyruvate kinase deficiency of red cells 2 OMIA 2 paths
- Sandhoff disease 2 OMIA 2 paths
- thyroid dyshormonogenesis 2A 2 OMIA 2 paths
- X-linked hypohidrotic ectodermal dysplasia 2 OMIA 2 paths
- X-linked myotubular myopathy 2 OMIA 2 paths
- familial adenomatous polyposis 1 1 OMIA 2 paths
- Marfan syndrome 1 OMIA 2 paths
- achromatopsia 2 1 OMIA 1 path
- achromatopsia 3 1 OMIA 1 path
- Alexander disease 1 OMIA 1 path
- autosomal recessive congenital ichthyosis 1 1 OMIA 1 path
- autosomal recessive congenital ichthyosis 6 1 OMIA 1 path
- autosomal recessive limb-girdle muscular dystrophy type 2F 1 OMIA 1 path
- autosomal recessive spastic paraplegia type 76 1 OMIA 1 path
- autosomal recessive spinocerebellar ataxia 13 1 OMIA 1 path
- Bernard-Soulier syndrome 1 OMIA 1 path
- complement component 3 deficiency 1 OMIA 1 path
- congenital factor VII deficiency 1 OMIA 1 path
- congenital myasthenic syndrome 5 1 OMIA 1 path
- congenital myasthenic syndrome 6 1 OMIA 1 path
- dilated cardiomyopathy 1A 1 OMIA 1 path
- EAST syndrome 1 OMIA 1 path
- Ehlers-Danlos syndrome due to tenascin-X deficiency 1 OMIA 1 path
- glycogen storage disease due to glucose-6-phosphatase deficiency type IA 1 OMIA 1 path
- glycogen storage disease III 1 OMIA 1 path
- glycogen storage disease VII 1 OMIA 1 path
- ichthyosis prematurity syndrome 1 OMIA 1 path
- leukocyte adhesion deficiency 3 1 OMIA 1 path
- microphthalmia, isolated, with coloboma 10 1 OMIA 1 path
- MONDO:0001741 1 OMIA 1 path
- MONDO:0002145 1 OMIA 1 path
- MONDO:0005147 1 OMIA 1 path
- MONDO:0005148 1 OMIA 1 path
- MONDO:0006527 1 OMIA 1 path
- MONDO:0006823 1 OMIA 1 path
- MONDO:0006825 1 OMIA 1 path
- MONDO:0007088 1 OMIA 1 path
- MONDO:0007290 1 OMIA 1 path
- MONDO:0007293 1 OMIA 1 path
- MONDO:0007417 1 OMIA 1 path
- MONDO:0007859 1 OMIA 1 path
- MONDO:0007868 1 OMIA 1 path
- MONDO:0008294 1 OMIA 1 path
- MONDO:0008593 1 OMIA 1 path
- MONDO:0008685 1 OMIA 1 path
- MONDO:0008713 1 OMIA 1 path
- MONDO:0008721 1 OMIA 1 path
- MONDO:0008729 1 OMIA 1 path
- MONDO:0008737 1 OMIA 1 path
- MONDO:0008746 1 OMIA 1 path
- MONDO:0008753 1 OMIA 1 path
- MONDO:0008762 1 OMIA 1 path
- MONDO:0008769 1 OMIA 1 path
- MONDO:0008770 1 OMIA 1 path
- MONDO:0008963 1 OMIA 1 path
- MONDO:0009020 1 OMIA 1 path
- MONDO:0009047 1 OMIA 1 path
- MONDO:0009111 1 OMIA 1 path
- MONDO:0009161 1 OMIA 1 path
- MONDO:0009292 1 OMIA 1 path
- MONDO:0009315 1 OMIA 1 path
- MONDO:0009459 1 OMIA 1 path
- MONDO:0009561 1 OMIA 1 path
- MONDO:0009606 1 OMIA 1 path
- MONDO:0009661 1 OMIA 1 path
- MONDO:0009756 1 OMIA 1 path
- MONDO:0009757 1 OMIA 1 path
- MONDO:0009758 1 OMIA 1 path
- MONDO:0009760 1 OMIA 1 path
- MONDO:0009823 1 OMIA 1 path
- MONDO:0009824 1 OMIA 1 path
- MONDO:0009916 1 OMIA 1 path
- MONDO:0010030 1 OMIA 1 path
- MONDO:0010041 1 OMIA 1 path
- MONDO:0010083 1 OMIA 1 path
- MONDO:0010099 1 OMIA 1 path
- MONDO:0010135 1 OMIA 1 path
- MONDO:0010188 1 OMIA 1 path
- MONDO:0010200 1 OMIA 1 path
- MONDO:0010311 1 OMIA 1 path
- MONDO:0010631 1 OMIA 1 path
- MONDO:0010730 1 OMIA 1 path
- MONDO:0010810 1 OMIA 1 path
- MONDO:0010977 1 OMIA 1 path
- MONDO:0011026 1 OMIA 1 path
- MONDO:0011066 1 OMIA 1 path
- MONDO:0011144 1 OMIA 1 path
- MONDO:0011158 1 OMIA 1 path
- MONDO:0011472 1 OMIA 1 path
- MONDO:0011493 1 OMIA 1 path
- MONDO:0011514 1 OMIA 1 path
- MONDO:0011680 1 OMIA 1 path
- MONDO:0011683 1 OMIA 1 path
- MONDO:0011827 1 OMIA 1 path
- MONDO:0011873 1 OMIA 1 path
- MONDO:0011968 1 OMIA 1 path
- MONDO:0012062 1 OMIA 1 path
- MONDO:0012220 1 OMIA 1 path
- MONDO:0012362 1 OMIA 1 path
- MONDO:0012414 1 OMIA 1 path
- MONDO:0012731 1 OMIA 1 path
- MONDO:0013066 1 OMIA 1 path
- MONDO:0013122 1 OMIA 1 path
- MONDO:0013131 1 OMIA 1 path
- MONDO:0013183 1 OMIA 1 path
- MONDO:0013227 1 OMIA 1 path
- MONDO:0013263 1 OMIA 1 path
- MONDO:0013271 1 OMIA 1 path
- MONDO:0013449 1 OMIA 1 path
- MONDO:0013595 1 OMIA 1 path
- MONDO:0013827 1 OMIA 1 path
- MONDO:0013924 1 OMIA 1 path
- MONDO:0014026 1 OMIA 1 path
- MONDO:0014351 1 OMIA 1 path
- MONDO:0014389 1 OMIA 1 path
- MONDO:0014421 1 OMIA 1 path
- MONDO:0014433 1 OMIA 1 path
- MONDO:0014436 1 OMIA 1 path
- MONDO:0014647 1 OMIA 1 path
- MONDO:0014811 1 OMIA 1 path
- MONDO:0014905 1 OMIA 1 path
- MONDO:0015008 1 OMIA 1 path
- MONDO:0016002 1 OMIA 1 path
- MONDO:0017576 1 OMIA 1 path
- MONDO:0017975 1 OMIA 1 path
- MONDO:0018881 1 OMIA 1 path
- MONDO:0019005 1 OMIA 1 path
- MONDO:0019149 1 OMIA 1 path
- MONDO:0019154 1 OMIA 1 path
- MONDO:0019353 1 OMIA 1 path
- MONDO:0019503 1 OMIA 1 path
- MONDO:0019567 1 OMIA 1 path
- MONDO:0019568 1 OMIA 1 path
- MONDO:0020040 1 OMIA 1 path
- MONDO:0020712 1 OMIA 1 path
- MONDO:0020723 1 OMIA 1 path
- MONDO:0030332 1 OMIA 1 path
- MONDO:0030512 1 OMIA 1 path
- MONDO:0030750 1 OMIA 1 path
- MONDO:0033092 1 OMIA 1 path
- MONDO:0042981 1 OMIA 1 path
- MONDO:0054780 1 OMIA 1 path
- MONDO:0060732 1 OMIA 1 path
- MONDO:0100250 1 OMIA 1 path
- MONDO:0100316 1 OMIA 1 path
- MONDO:0700239 1 OMIA 1 path
- MONDO:0800405 1 OMIA 1 path
- MONDO:0859311 1 OMIA 1 path
- MONDO:1010459 1 OMIA 1 path
- MONDO:1010520 1 OMIA 1 path
- MONDO:1010640 1 OMIA 1 path
- MONDO:1010644 1 OMIA 1 path
- MONDO:1010666 1 OMIA 1 path
- MONDO:1010671 1 OMIA 1 path
- MONDO:1010716 1 OMIA 1 path
- MONDO:1010717 1 OMIA 1 path
- MONDO:1010718 1 OMIA 1 path
- MONDO:1010746 1 OMIA 1 path
- MONDO:1010747 1 OMIA 1 path
- MONDO:1010785 1 OMIA 1 path
- MONDO:1010794 1 OMIA 1 path
- MONDO:1010796 1 OMIA 1 path
- MONDO:1010833 1 OMIA 1 path
- MONDO:1010851 1 OMIA 1 path
- MONDO:1010864 1 OMIA 1 path
- MONDO:1010869 1 OMIA 1 path
- MONDO:1010870 1 OMIA 1 path
- MONDO:1010884 1 OMIA 1 path
- MONDO:1010924 1 OMIA 1 path
- MONDO:1010950 1 OMIA 1 path
- MONDO:1011031 1 OMIA 1 path
- MONDO:1011100 1 OMIA 1 path
- MONDO:1011207 1 OMIA 1 path
- MONDO:1011209 1 OMIA 1 path
- MONDO:1011264 1 OMIA 1 path
- MONDO:1011277 1 OMIA 1 path
- MONDO:1011282 1 OMIA 1 path
- MONDO:1011285 1 OMIA 1 path
- MONDO:1011435 1 OMIA 1 path
- MONDO:1011556 1 OMIA 1 path
- MONDO:1012055 1 OMIA 1 path
- MONDO:1012266 1 OMIA 1 path
- MONDO:1012272 1 OMIA 1 path
- MONDO:1012392 1 OMIA 1 path
- MONDO:1012419 1 OMIA 1 path
- MONDO:1012492 1 OMIA 1 path
- MONDO:1012517 1 OMIA 1 path
- MONDO:1012529 1 OMIA 1 path
- MONDO:1012606 1 OMIA 1 path
- MONDO:1012607 1 OMIA 1 path
- MONDO:1012613 1 OMIA 1 path
- MONDO:1012649 1 OMIA 1 path
- MONDO:1012658 1 OMIA 1 path
- MONDO:1012662 1 OMIA 1 path
- MONDO:1012699 1 OMIA 1 path
- MONDO:1012700 1 OMIA 1 path
- MONDO:1012707 1 OMIA 1 path
- MONDO:1012742 1 OMIA 1 path
- MONDO:1012748 1 OMIA 1 path
- MONDO:1012764 1 OMIA 1 path
- MONDO:1012786 1 OMIA 1 path
- MONDO:1012789 1 OMIA 1 path
- MONDO:1012809 1 OMIA 1 path
- MONDO:1012814 1 OMIA 1 path
- MONDO:1012816 1 OMIA 1 path
- MONDO:1012818 1 OMIA 1 path
- MONDO:1012859 1 OMIA 1 path
- MONDO:1012879 1 OMIA 1 path
- MONDO:1012921 1 OMIA 1 path
- MONDO:1012930 1 OMIA 1 path
- MONDO:1012935 1 OMIA 1 path
- MONDO:7770054 1 OMIA 1 path
- MONDO:7770109 1 OMIA 1 path
- MONDO:7770231 1 OMIA 1 path
- MONDO:7770247 1 OMIA 1 path
- MONDO:7770256 1 OMIA 1 path
- MONDO:7770328 1 OMIA 1 path
- MONDO:7770373 1 OMIA 1 path
- MONDO:7770454 1 OMIA 1 path
- MONDO:7770500 1 OMIA 1 path
- MONDO:7770608 1 OMIA 1 path
- MONDO:7770609 1 OMIA 1 path
- MONDO:7770643 1 OMIA 1 path
- mucopolysaccharidosis type 3A 1 OMIA 1 path
- myeloperoxidase deficiency 1 OMIA 1 path
- myostatin-related muscle hypertrophy 1 OMIA 1 path
- nemaline myopathy 2 1 OMIA 1 path
- neuronal ceroid lipofuscinosis 1 1 OMIA 1 path
- neuronal ceroid lipofuscinosis 5 1 OMIA 1 path
- neuronal ceroid lipofuscinosis 8 1 OMIA 1 path
- neuropathy, hereditary sensory and autonomic, type 2B 1 OMIA 1 path
- osteogenesis imperfecta type 10 1 OMIA 1 path
- palmoplantar keratoderma, nonepidermolytic, focal 1 1 OMIA 1 path
- Pelizaeus-Merzbacher spectrum disorder 1 OMIA 1 path
- pituitary hormone deficiency, combined, 1 1 OMIA 1 path
- platelet-type bleeding disorder 18 1 OMIA 1 path
- platelet-type bleeding disorder 8 1 OMIA 1 path
- primary ciliary dyskinesia 14 1 OMIA 1 path
- pyruvate dehydrogenase phosphatase deficiency 1 OMIA 1 path
- retinitis pigmentosa 28 1 OMIA 1 path
- retinitis pigmentosa 43 1 OMIA 1 path
- retinitis pigmentosa 51 1 OMIA 1 path
- Scott syndrome 1 OMIA 1 path
- Senior-Loken syndrome 4 1 OMIA 1 path
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive 1 OMIA 1 path
- thyroid dyshormonogenesis 1 1 OMIA 1 path
- van den Ende-Gupta syndrome 1 OMIA 1 path
- X-linked Alport syndrome 1 OMIA 1 path
- xanthinuria type II 1 OMIA 1 path
- hereditary neoplastic syndrome 3 paths
- colon carcinoma 2 paths
- complex neurodevelopmental disorder 2 paths
- Noonan syndrome 2 paths
- RASopathy 2 paths
- AGAT deficiency 1 path
- autism 1 path
- cardiofaciocutaneous syndrome 1 path
- cardiofaciocutaneous syndrome 1 1 path
- CEBALID syndrome 1 path
- central core myopathy 1 path
- classic familial adenomatous polyposis 1 path
- cognitive impairment with or without cerebellar ataxia 1 path
- congenital fiber-type disproportion myopathy 1 path
- congenital multicore myopathy with external ophthalmoplegia 1 path
- Cowden disease 1 path
- Cowden syndrome 1 1 path
- developmental and epileptic encephalopathy 1 path
- developmental and epileptic encephalopathy, 11 1 path
- developmental and epileptic encephalopathy, 13 1 path
- DICER1-related tumor predisposition 1 path
- dilated cardiomyopathy 1NN 1 path
- Dravet syndrome 1 path
- early-infantile DEE 1 path
- endometrial carcinoma 1 path
- familial meningioma 1 path
- familial thoracic aortic aneurysm and aortic dissection 1 path
- Fanconi renotubular syndrome 1 1 path
- Gardner syndrome 1 path
- gastric neoplasm 1 path
- generalized epilepsy with febrile seizures plus 1 path
- generalized epilepsy with febrile seizures plus, type 2 1 path
- glioma susceptibility 2 1 path
- global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome 1 path
- goiter, multinodular 1, with or without Sertoli-Leydig cell tumors 1 path
- hemimegalencephaly 1 path
- hepatocellular carcinoma 1 path
- hereditary von Willebrand disease 1 path
- intellectual disability 1 path
- intestinal polyp 1 path
- isolated focal cortical dysplasia type II 1 path
- King-Denborough syndrome 1 path
- LEOPARD syndrome 2 1 path
- LEOPARD syndrome 3 1 path
- Lhermitte-Duclos disease 1 path
- lung carcinoma 1 path
- macrocephaly-autism syndrome 1 path
- malignant hyperthermia of anesthesia 1 path
- malignant hyperthermia, susceptibility to, 1 1 path
- migraine, familial hemiplegic, 3 1 path
- myoclonus, familial, 2 1 path
- Noonan syndrome 1 1 path
- Noonan syndrome 5 1 path
- Noonan syndrome 7 1 path
- Noonan syndrome and Noonan-related syndrome 1 path
- Noonan syndrome with multiple lentigines 1 path
- overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes 1 path
- periampullary adenoma 1 path
- pleuropulmonary blastoma 1 path
- polymicrogyria 1 path
- prostate cancer 1 path
- prostate cancer, hereditary 1 path
- Proteus-like syndrome 1 path
- PTEN hamartoma tumor syndrome 1 path
- pulmonary arterial hypertension 1 path
- pulmonary hypertension, primary, 1 1 path
- pulmonary venoocclusive disease 1 1 path
- RYR1-related myopathy 1 path
- scoliosis 1 path
- segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome 1 path
- seizures, benign familial infantile, 3 1 path
- seizures, benign familial infantile, 5 1 path
- stomach polyp 1 path
- thrombocytopenia 1 path
- VACTERL with hydrocephalus 1 path
- von Willebrand disease 1 1 path
- von Willebrand disease 2 1 path
- von Willebrand disease 3 1 path
- von Willebrand disease type 2A 1 path
- von Willebrand disease type 2B 1 path
- von Willebrand disease type 2M 1 path
- von Willebrand disease type 2N 1 path