Disease groups
2,194 disease groups, by OMIA group number.
| OMIA group | Name | Species | The chain reached | Best score |
|---|---|---|---|---|
| 497 | Hyperbilirubinaemia II | 1 | Human disease | 9.0 |
| 498 | Hyperbilirubinaemia II-like | 1 | Animal disease only | |
| 499 | Hypercholesterolaemia | 7 | Target evidence | 65.5 |
| 502 | Hypereosinophilic syndrome | 4 | Human disease | 37.5 |
| 503 | Hyperkinesis | 1 | Animal disease only | |
| 506 | Hypermetria | 1 | Animal disease only | |
| 507 | Hyperostosis | 1 | Human disease | 9.0 |
| 508 | Hyperparathyroidism | 4 | Human disease | 40.0 |
| 509 | Hypertension | 3 | Animal disease only | |
| 510 | Hypertension, essential | 1 | Human disease | 31.5 |
| 511 | Hyperthyroidism | 4 | Human disease | 15.0 |
| 513 | Hypertrichosis | 2 | Human disease | 29.5 |
| 514 | Hypertriglyceridaemia | 2 | Human disease | 12.0 |
| 515 | Cardiomyopathy, hypertrophic | 8 | Human disease | 37.5 |
| 518 | Neuropathy, hypertrophic | 1 | Animal disease only | |
| 519 | Hypoadrenocorticism | 4 | Human disease | 40.0 |
| 520 | Hypoadrenocorticism, primary | 2 | Animal disease only | |
| 522 | Hypogonadism | 2 | Human disease | 34.5 |
| 525 | Hypomandibular furrow closure | 1 | Animal disease only | |
| 526 | Hypomyelination of the central nervous system | 3 | Animal disease only | |
| 527 | Hypomyelinogenesis, congenital | 4 | Animal disease only | |
| 528 | Hypoparathyroidism | 3 | Human disease | 30.0 |
| 529 | Hypoplasia of mammary gland, congenital | 1 | Animal disease only | |
| 530 | Hypoplasia of sex organs | 1 | Animal disease only | |
| 534 | Hyposelenaemia-hyperselenaemia | 1 | Animal disease only | |
| 535 | Hypothalamic dysplasia | 1 | Animal disease only | |
| 536 | Hypothyroidism, congenital | 8 | Human gene | 40.0 |
| 537 | Hypothyroidism and dwarfism | 1 | Animal disease only | |
| 538 | Hypothyroidism, primary | 2 | Animal disease only | |
| 540 | Hypotrichosis, generic | 12 | Human disease | 15.0 |
| 541 | Hypotrichosis, semi | 1 | Animal disease only | |
| 542 | Hypotrichosis, streaked | 1 | Human gene | 29.0 |
| 543 | Hypohidrotic ectodermal dysplasia, X-linked, EDA-related | 4 | Target evidence | 85.0 |
| 544 | Hypotrichosis with thymic aplasia, congenital | 1 | Animal disease only | |
| 545 | Axonopathy, hypotrophic | 1 | Human disease | 9.0 |
| 546 | Ichthyosis, TGM1-related | 1 | Human gene | 34.0 |
| 550 | Immunodeficiency | 3 | Human disease | 37.5 |
| 551 | Immunoglobulin 7S deficiency | 1 | Animal disease only | |
| 552 | Immunoglobulin A deficiency | 2 | Human disease | 9.5 |
| 553 | Immunoglobulin A glomerulonephropathy | 1 | Animal disease only | |
| 554 | Immunoglobulin G deficiency | 3 | Animal disease only | |
| 555 | Immunoglobulin G2 deficiency | 1 | Animal disease only | |
| 556 | Immunoglobulin M deficiency | 2 | Human disease | 9.0 |
| 559 | Imperforate anus with rectovaginal fistula | 3 | Animal disease only | |
| 560 | Impotentia cocundi | 2 | Animal disease only | |
| 561 | Inborn error of hepatic metabolism | 1 | Animal disease only | |
| 562 | Infertility | 5 | Animal disease only | |
| 563 | Interdigital tissue pachydermia | 1 | Animal disease only | |
| 564 | Difference of sexual development, generic | 24 | Human disease | 15.0 |
| 565 | Intestinal cobalamin malabsorption, AMN-related | 1 | Target evidence | 54.3 |