Comparative

Disease groups

2,194 disease groups, by OMIA group number.

OMIA group Name Species The chain reached Best score
1409 Lymphoproliferative disease 1 Animal disease only
1410 Diphallus 1 Animal disease only
1411 Anotia 2 Human disease 9.5
1412 Hyperextension, lower limb 2 Animal disease only
1413 Retinitis pigmentosa 2 Human disease 31.5
1415 Hyperkeratosis, epidermolytic 2 Target evidence 57.5
1417 Pulmonary fibrosis, idiopathic 2 Human disease 12.0
1418 Cricopharyngeal dysfunction 1 Animal disease only
1419 Aortic aneurysm, familial thoracic 1 Animal disease only
1420 Retinal dysplasia and persistent primary vitreous 1 Animal disease only
1422 Chylothorax 2 Human disease 12.0
1424 Casein, beta, absence of 1 Animal disease only
1427 Gangliosidosis, GM2, (AB variant), GM2A-related 2 Target evidence 62.7
1428 Trapped Neutrophil Syndrome 1 Target evidence 59.2
1431 Vitamin D-deficiency rickets, type II 2 Drug 63.2
1432 Retinal atrophy - Cone-rod dystrophy 4 1 Target evidence 55.0
1436 Non-shivering thermiogenesis, absence of 1 Animal disease only
1437 Lactoglobulin, beta, aberrant low expression 1 Animal disease only
1438 Coat colour, silver 2 Animal disease only
1441 Osteosarcoma 4 Human disease 37.5
1442 Forelimb-girdle muscular anomaly 1 Animal disease only
1443 Neuronal ceroid lipofuscinosis, 6 3 Target evidence 69.4
1444 Multifocal retinopathy 1 1 Target evidence 58.6
1448 Spondyloepiphyseal dysplasia, congenital type 1 Human disease 9.0
1450 Congenital muscular dystonia 1 1 Drug 63.4
1451 Congenital muscular dystonia 2 1 Target evidence 55.7
1452 Tail, crooked 1 Animal disease only
1455 Retinal atrophy - Cone-rod dystrophy, NPHP4-related 1 Target evidence 59.5
1456 Recurrent airway obstruction 1 Human disease 9.0
1457 Multiple acyl-CoA dehydrogenase deficiency 2 Human disease 12.0
1458 Hypotrichosis, juvenile with age-dependent emphysema 1 Human disease 9.0
1461 Gangliosidosis, GM2, type I (B variant) 7 Target evidence 85.2
1462 Gangliosidosis, GM2, type II (Sandhoff or variant 0) 3 Target evidence 89.3
1463 Heterotopia, subcortical, unilateral 1 Animal disease only
1464 Pseudomyotonia, congenital 2 Drug 63.4
1465 Arthrogryposis multiplex congenita, generic 3 Animal disease only
1466 Exercise-induced collapse 1 Target evidence 54.5
1467 Neuropathy, sensory ataxic 1 Animal disease only
1468 Multiple system degeneration, SERAC1-related 1 Target evidence 58.1
1470 Meningoencephalitis 1 Human disease 6.5
1471 Neonatal encephalopathy with seizures, ATF2-related 1 Animal disease only
1472 Neuronal ceroid lipofuscinosis, 2 3 Target evidence 92.0
1473 Dwarfism, growth-hormone deficiency 3 Target evidence 50.3
1474 Rupture of the cranial cruciate ligament, predisposition to 1 Animal disease only
1476 Collagenosis, reactive perforating 1 Human disease 9.0
1478 Skin wound healing 1 Animal disease only
1480 Melanoma, Melanoma-bearing Libĕchov Minipig (MeLiM) 1 Animal disease only
1481 Achromatopsia-2, CNGA3-related 2 Target evidence 61.8
1482 Neuronal ceroid lipofuscinosis, 5 3 Target evidence 69.2
1483 Osteogenesis imperfecta, SERPINH1-related 1 Target evidence 59.0