Disease groups
2,194 disease groups, by OMIA group number.
| OMIA group | Name | Species | The chain reached | Best score |
|---|---|---|---|---|
| 146 | Brachydactyly | 4 | Human disease | 12.5 |
| 147 | Brachygnathia | 10 | Animal disease only | |
| 149 | Brachygnathia superior | 9 | Animal disease only | |
| 150 | Brachygnathia superior and degenerative joint disease | 1 | Animal disease only | |
| 151 | Brachyspina | 1 | Target evidence | 58.0 |
| 153 | Brown rippled | 1 | Animal disease only | |
| 155 | C3 deficiency | 3 | Drug | 69.5 |
| 156 | C8 deficiency | 1 | Human gene | 34.0 |
| 157 | Intervertebral disc disease, predisposition to | 11 | Animal disease only | |
| 158 | Calcinosis circumscripta | 2 | Animal disease only | |
| 159 | Cardiac anomaly | 2 | Animal disease only | |
| 160 | Cardiomyopathy | 9 | Human disease | 37.5 |
| 161 | Cardiomyopathy and woolly haircoat syndrome | 1 | Animal disease only | |
| 162 | Cardiomyopathy, dilated | 11 | Drug | 53.6 |
| 164 | Cardiomyopathy, spontaneous | 1 | Animal disease only | |
| 165 | Cardiovascular malformations | 1 | Animal disease only | |
| 166 | Carpal subluxation | 1 | Animal disease only | |
| 168 | Cataract, generic | 29 | Animal disease only | |
| 170 | Cauda equina syndrome | 1 | Human disease | 26.5 |
| 172 | Central core myopathy | 2 | Human disease | 22.0 |
| 173 | Cephalothoracophagus | 1 | Animal disease only | |
| 174 | Cerebellar Purkinje cell degeneration | 1 | Animal disease only | |
| 175 | Cerebellar abiotrophy | 9 | Human gene | 35.0 |
| 176 | Cerebellar anomaly, congenital | 2 | Animal disease only | |
| 177 | Cerebellar cortical atrophy | 4 | Animal disease only | |
| 178 | Cerebellar disease | 1 | Animal disease only | |
| 179 | Cerebellar hypoplasia | 6 | Human disease | 15.0 |
| 181 | Neuronal Ceroid Lipofuscinosis, generic | 12 | Animal disease only | |
| 185 | Chediak-Higashi syndrome | 5 | Target evidence | 74.9 |
| 187 | Chondrodysplasia, generic | 5 | Animal disease only | |
| 189 | Chondrodystrophy | 8 | Human disease | 12.5 |
| 192 | Chronic interstitial nephropathy | 1 | Animal disease only | |
| 194 | Citrullinaemia | 2 | Target evidence | 76.9 |
| 195 | Claw/hoof disorders | 5 | Animal disease only | |
| 197 | Cleft palate | 11 | Human disease | 15.0 |
| 198 | Clubbed down | 1 | Animal disease only | |
| 202 | Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related | 33 | Drug | 67.4 |
| 204 | Coat colour, albinism, incomplete | 1 | Animal disease only | |
| 209 | Coat colour, dominant white | 13 | Drug | 63.1 |
| 211 | Coat colour, merle | 1 | Animal disease only | |
| 212 | Coat colour, pink-eyed dilution | 6 | Animal disease only | |
| 214 | Coat colour, white spotting | 7 | Target evidence | 57.1 |
| 218 | Choroidal hypoplasia, NHEJ1-related | 1 | Animal disease only | |
| 219 | Coloboma | 9 | Human disease | 15.0 |
| 220 | Severe combined immunodeficiency disease, autosomal, PRKDC-related | 2 | Drug | 60.8 |
| 224 | Conotruncal heart malformations | 1 | Human disease | 9.0 |
| 225 | Contact activation defect | 1 | Animal disease only | |
| 226 | Copper deficiency, congenital | 1 | Animal disease only | |
| 227 | Cor triatriatum dexter | 1 | Human disease | 6.5 |
| 229 | Corneal dermoid | 2 | Animal disease only |