Disease groups
2,194 disease groups, by OMIA group number.
| OMIA group | Name | Species | The chain reached | Best score |
|---|---|---|---|---|
| 356 | Eye balls, lack of | 1 | Animal disease only | |
| 358 | Eye defects | 9 | Animal disease only | |
| 359 | Eyelid gland, third, prolapse of | 2 | Animal disease only | |
| 360 | Facial digital syndrome | 1 | Human disease | 9.0 |
| 361 | Factor VII deficiency | 2 | Drug | 84.2 |
| 362 | Factor X deficiency | 2 | Human disease | 17.0 |
| 363 | Factor XI deficiency | 3 | Drug | 69.4 |
| 364 | Factor XII deficiency | 4 | Drug | 71.1 |
| 365 | Faded shaker | 1 | Animal disease only | |
| 366 | Fanconi syndrome | 4 | Target evidence | 63.7 |
| 368 | Feather colour, generic | 47 | Animal disease only | |
| 369 | Feather colour, oculocutaneous albinism type I (OCA1), TYR-related | 6 | Drug | 61.4 |
| 370 | Feather colour, SLC45A2-related | 6 | Target evidence | 66.6 |
| 377 | Feather curling | 1 | Animal disease only | |
| 378 | Feather hypoplasia | 1 | Animal disease only | |
| 379 | Feather colour, lethal | 1 | Animal disease only | |
| 380 | Feathering, Z-linked | 3 | Animal disease only | |
| 388 | Fibrodysplasia ossificans | 3 | Drug | 85.6 |
| 389 | Focal metatarsal fistula | 1 | Animal disease only | |
| 391 | Chromosomal structural anomaly, fragile site, sex-chromosome | 3 | Human disease | 35.0 |
| 392 | Chromosomal structural anomaly, fragile site, autosomal | 10 | Human disease | 15.0 |
| 393 | Tetragametic chimerism (including Freemartin) | 10 | Animal disease only | |
| 394 | Frizzle, KRT6A-related | 1 | Human gene | 21.0 |
| 396 | Fucosidosis, alpha | 2 | Target evidence | 61.2 |
| 397 | Fur deficiency | 1 | Animal disease only | |
| 398 | Furloss | 1 | Animal disease only | |
| 400 | Galactosialidosis | 1 | Human disease | 9.0 |
| 401 | Gangliosidosis, generic | 5 | Animal disease only | |
| 402 | Gangliosidosis, GM1 | 5 | Target evidence | 64.7 |
| 403 | Gangliosidosis, GM2, generic | 3 | Animal disease only | |
| 404 | Gastric dilatation volvulus syndrome | 4 | Human disease | 15.0 |
| 405 | Gaucher disease, generic | 3 | Human disease | 40.0 |
| 406 | Genital hypoplasia | 1 | Animal disease only | |
| 409 | Gingival hypertrophy | 2 | Human disease | 9.5 |
| 410 | Glandular aplasia | 1 | Animal disease only | |
| 411 | Glaucoma, generic | 8 | Human disease | 15.0 |
| 412 | Cloaca | 2 | Animal disease only | |
| 413 | Glomerulonephritis | 2 | Human disease | 12.0 |
| 414 | Glomerulonephropathy | 1 | Animal disease only | |
| 415 | Glossopharyngeal defect | 1 | Animal disease only | |
| 416 | Glucose-6-phosphate dehydrogenase deficiency | 3 | Human disease | 15.0 |
| 418 | Glycogen storage disease Ia | 1 | Target evidence | 82.9 |
| 419 | Glycogen storage disease II | 6 | Drug | 61.3 |
| 420 | Glycogen storage disease IV | 3 | Target evidence | 69.7 |
| 421 | Glycogen storage disease VII | 1 | Target evidence | 77.6 |
| 422 | Glyoxalase II deficiency | 1 | Human disease | 6.5 |
| 424 | Goitre, familial | 11 | Human gene | 40.0 |
| 426 | Gonadal hypoplasia | 2 | Animal disease only | |
| 427 | Granule cell type cerebellar hypoplasia | 1 | Animal disease only | |
| 428 | Haemochromatosis | 10 | Human disease | 15.0 |