Disease groups
1,086 disease groups whose chain reached a human disease, by OMIA group number.
| OMIA group | Name | Species | The chain reached | Best score |
|---|---|---|---|---|
| 1166 | Priapism | 2 | Human disease | 12.0 |
| 1168 | Coronal suture synostosis | 1 | Human disease | 9.0 |
| 1169 | Ascites | 5 | Human disease | 15.0 |
| 1171 | Methaemoglobinaemia, generic | 1 | Human disease | 9.0 |
| 1172 | Genu valgum | 1 | Human disease | 9.0 |
| 1173 | Patent ductus venosus | 2 | Human disease | 9.5 |
| 1174 | Synovial chondromatosis | 2 | Human disease | 12.0 |
| 1175 | Porphyria, congenital erythropoietic | 4 | Target evidence | 89.8 |
| 1176 | Porphyria cutanea tarda | 2 | Target evidence | 60.9 |
| 1177 | Polyuria | 2 | Human disease | 12.0 |
| 1178 | Stomatocytosis and gastritis | 1 | Human disease | 9.0 |
| 1179 | Polyglandular autoimmune syndrome, type II | 1 | Human disease | 9.0 |
| 1181 | Atrial fibrillation | 3 | Human disease | 37.0 |
| 1183 | Bullous pemphigoid | 5 | Human disease | 37.5 |
| 1184 | Hypophosphataemia | 2 | Human disease | 37.0 |
| 1185 | Retinoschisis | 2 | Human disease | 27.0 |
| 1186 | Erythrocytosis | 2 | Human disease | 12.0 |
| 1187 | Hypospadias | 6 | Human disease | 15.0 |
| 1188 | Pemphigus | 5 | Human disease | 40.0 |
| 1189 | Lymphangiectasia | 1 | Human disease | 14.0 |
| 1191 | Hemivertebrae | 3 | Human disease | 15.0 |
| 1194 | Wolff-Parkinson-White syndrome | 3 | Human disease | 45.0 |
| 1196 | Hypergammaglobulinaemia | 1 | Human disease | 9.0 |
| 1197 | Horner syndrome | 4 | Human disease | 15.0 |
| 1200 | Tremor, high-frequency | 2 | Drug | 62.5 |
| 1202 | Scleroderma | 1 | Human disease | 9.0 |
| 1203 | Budd-chiari syndrome | 2 | Human disease | 12.0 |
| 1205 | Pseudocholinesterase deficiency | 1 | Human disease | 9.0 |
| 1207 | Neuropathy, giant axonal | 2 | Human disease | 12.0 |
| 1208 | Alexander disease | 2 | Target evidence | 87.5 |
| 1210 | Hyperlipoproteinaemia | 3 | Human disease | 40.0 |
| 1213 | Premature senesence | 2 | Target evidence | 83.0 |
| 1214 | Osteochondromatosis, EXT2-related | 1 | Target evidence | 58.0 |
| 1217 | Meckel diverticulum | 1 | Human disease | 9.0 |
| 1218 | Persistent truncus arteriosus with ventricular septal defect and patent foramen ovale | 1 | Human disease | 9.0 |
| 1219 | Dermatosis | 1 | Human disease | 24.0 |
| 1220 | Vasculopathy, cutaneous and renal | 1 | Human disease | 24.0 |
| 1221 | Cerebellar degeneration | 4 | Human disease | 27.5 |
| 1222 | Leber congenital amaurosis | 2 | Drug | 63.3 |
| 1223 | Goniodysgenesis | 1 | Human gene | 29.0 |
| 1224 | Craniosynostosis | 1 | Human disease | 9.0 |
| 1227 | Intussusception, predisposition to | 10 | Human disease | 15.0 |
| 1228 | Spherocytosis | 3 | Target evidence | 63.7 |
| 1229 | Haemophagocytic syndrome | 2 | Human disease | 12.0 |
| 1230 | XY sex reversal, SRY-related | 6 | Target evidence | 68.8 |
| 1231 | Hyperhidrosis | 1 | Human disease | 9.0 |
| 1238 | Coeliac sprue | 1 | Human disease | 9.0 |
| 1239 | Epiphora | 1 | Human disease | 6.5 |
| 1240 | Hyperphosphatasaemia | 1 | Human disease | 9.0 |
| 1243 | Alkaptonuria | 6 | Target evidence | 89.6 |