Comparative

Disease groups

2,194 disease groups, by OMIA group number.

OMIA group Name Species The chain reached Best score
1245 Retinal degeneration I 1 Human disease 9.0
1246 Chronic valvular disease 1 Animal disease only
1247 Spinal dysmyelination 1 Target evidence 59.7
1248 Mucolipidosis II 1 Human disease 24.0
1253 Pop-eye 1 Animal disease only
1254 Diplopodia-4 1 Animal disease only
1255 Placental anastomoses 1 Animal disease only
1256 Woolly hair 2 Human disease 6.5
1257 Renal cysts 1 Animal disease only
1258 Obesity 7 Target evidence 41.8
1260 Retinal atrophy - Rod-cone dysplasia 2, RD3-related 1 Human disease 9.0
1261 Gluten-sensitive enteropathy 1 Human disease 9.0
1262 Feather colour, black at hatch 1 Animal disease only
1264 Hydromelia 1 Human disease 9.0
1265 Preputial prolapse/eversion 1 Animal disease only
1266 Otitis media, predisposition to 8 Human disease 15.0
1267 Cranial cruciate ligament deficiency, congenital 1 Animal disease only
1268 Pheochromocytoma 2 Human disease 37.0
1269 Hyperaldosteronism 1 Human disease 9.0
1270 Convulsions and ataxia, CACNA1A-related 1 Drug 73.5
1271 Dwarfism, ACAN-related 3 Target evidence 61.3
1272 Comedo syndrome 1 Human disease 9.0
1273 Fasciola gigantica, susceptibility/resistance to 1 Animal disease only
1274 Coat colour, black crystal 1 Animal disease only
1276 Facial eczema 2 Animal disease only
1277 Otitis interna, predisposition to 3 Animal disease only
1278 Hypotrichosis, dominant 2 Human disease 32.0
1279 Hypotrichosis, recessive 2 Animal disease only
1280 Polioencephalomyelopathy 1 Animal disease only
1282 Neuronopathy, progressive 1 Animal disease only
1283 Xanthinuria, generic 5 Human disease 15.0
1284 Feathering, inhibited 1 Animal disease only
1286 Evans syndrome 1 Human disease 21.5
1287 Keratitis 3 Human disease 15.0
1288 Feather colour, dilute down lethal 1 Animal disease only
1289 Urticaria pigmentosa 1 Human disease 29.0
1290 Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome 1 Human disease 9.0
1292 Polyneuropathy, generic 2 Human disease 12.0
1294 Dwarfism, growth-hormone-receptor deficiency 1 Human disease 34.0
1296 Dwarfism, hypochondroplastic 1 Animal disease only
1297 Early retinal degeneration 1 Animal disease only
1298 Progressive rod-cone degeneration, PRCD-related 1 Human gene 29.0
1299 Avian sarcoma and leukosis virus, subgroup A, susceptibility/resistance to 1 Human disease 9.0
1300 Hereditary multiple malformation 1 Animal disease only
1301 Hernia, peritoneopericardial 1 Animal disease only
1302 Avian sarcoma and leukosis virus, subgroup B, susceptibility/resistance to 1 Human disease 34.0
1303 Neuronal vacuolar disorder 1 Animal disease only
1304 Yellow-semen syndrome 1 Animal disease only
1307 Palmar/plantar osteochondral fragments 1 Animal disease only
1309 Mucopolysaccharidosis IIIA 1 Target evidence 84.4