Comparative

Disease groups

2,194 disease groups, by OMIA group number.

OMIA group Name Species The chain reached Best score
1548 Wingless, sex-linked 1 Animal disease only
1549 Wingless, Japanese 1 Animal disease only
1550 Wingless with scoliosis 1 Animal disease only
1551 Brachycephaly 8 Target evidence 51.4
1552 Neuronal ceroid lipofuscinosis, 12 2 Target evidence 61.5
1553 Multifocal retinopathy 2 1 Target evidence 58.6
1554 Multifocal retinopathy 3 1 Target evidence 58.6
1556 Ankylosis, jaw 1 Animal disease only
1557 Ljutikow's lethal 1 Animal disease only
1558 Micromelia, achondroplastic 1 Animal disease only
1561 Periodic Fever Syndrome 1 Target evidence 26.9
1562 Pulmonary hypoplasia with anasarca, ADAMTS3-related 2 Human gene 32.0
1563 Sebaceous adenitis 1 Animal disease only
1564 Bleeding disorder, P2RY12-related 1 Drug 62.0
1565 Abortion and stillbirth, MIMT1-related 1 Animal disease only
1567 Hypercholesterolaemia, Kurosawa and Kusanagi 1 Animal disease only
1568 Narrow axis 1 Animal disease only
1570 Persistent right aortic arch, with subclavian artery and ligamentum arteriosum 1 Animal disease only
1572 Retinal atrophy, progressive, SLC4A3-related 1 Animal disease only
1573 Leukaemia, chronic monocytic 1 Drug 82.8
1574 Severe combined immunodeficiency disease, autosomal, T cell-negative, B cell-negative, NK cell-positive 3 Target evidence 62.0
1575 Retinal atrophy - Rod-cone dysplasia 4 1 Human gene 34.0
1577 Glycogen storage disease IIIa 1 Target evidence 63.1
1578 Immunodeficiency syndrome, SLC5A3-related 1 Animal disease only
1583 Hypotrichosis, with whiskers short and curled 1 Human disease 9.0
1585 Cleft lip and jaw, unilateral 1 Animal disease only
1586 Deficient acetaminophen glucuronidation 1 Animal disease only
1588 Ichthyosis, PNPLA1-related 1 Human gene 29.0
1589 Anal furunculosis 1 Animal disease only
1592 Episodic falling, BCAN-related 1 Animal disease only
1594 Hyperekplexia (Startle disease), SLC6A5-related 1 Target evidence 60.7
1595 Growth disorder, syndromic, OBSL1-related 2 Human gene 32.0
1596 Epilepsy, benign familial juvenile, LGI2-related 1 Animal disease only
1597 Coat colour, English spotting 1 Animal disease only
1601 XY difference of sexual development, generic 6 Human disease 15.0
1604 Feather, curly 1 Animal disease only
1606 Neuroaxonal dystrophy with cerebellar abiotrophy 1 Animal disease only
1607 Skin colour 78 Animal disease only
1608 May-Hegglin anomaly 1 Target evidence 74.0
1609 Exfoliative cutaneous lupus erythematosus 1 Animal disease only
1612 Oligozeugodactyly 1 Target evidence 52.2
1613 Retinal dystrophy, early onset, Bengal 1 Animal disease only
1614 Vitamin D-deficiency rickets, non-type I, non-type II 1 Animal disease only
1616 Chondrodysplasia, "llama syndrome" 1 Animal disease only
1617 Sweet taste, lack of 3 Animal disease only
1619 Muscular dystrophy, congenital merosin-deficient 1 Human disease 9.0
1620 Muscular dystrophy, limb-girdle, type R4 (LGMDR4) 1 Animal disease only
1621 Muscular dystrophy-dystroglycanopathy (limb-girdle) 2 Human gene 32.0
1622 Avian sarcoma and leukosis virus, subgroup C, susceptibility/resistance to 1 Animal disease only
1623 Casein, alpha-S2, absence 1 Animal disease only