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 |
|---|---|---|---|---|
| 497 | Hyperbilirubinaemia II | 1 | Human disease | 9.0 |
| 499 | Hypercholesterolaemia | 7 | Target evidence | 65.5 |
| 502 | Hypereosinophilic syndrome | 4 | Human disease | 37.5 |
| 507 | Hyperostosis | 1 | Human disease | 9.0 |
| 508 | Hyperparathyroidism | 4 | Human disease | 40.0 |
| 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 |
| 519 | Hypoadrenocorticism | 4 | Human disease | 40.0 |
| 522 | Hypogonadism | 2 | Human disease | 34.5 |
| 528 | Hypoparathyroidism | 3 | Human disease | 30.0 |
| 536 | Hypothyroidism, congenital | 8 | Human gene | 40.0 |
| 540 | Hypotrichosis, generic | 12 | Human disease | 15.0 |
| 542 | Hypotrichosis, streaked | 1 | Human gene | 29.0 |
| 543 | Hypohidrotic ectodermal dysplasia, X-linked, EDA-related | 4 | Target evidence | 85.0 |
| 545 | Axonopathy, hypotrophic | 1 | Human disease | 9.0 |
| 546 | Ichthyosis, TGM1-related | 1 | Human gene | 34.0 |
| 550 | Immunodeficiency | 3 | Human disease | 37.5 |
| 552 | Immunoglobulin A deficiency | 2 | Human disease | 9.5 |
| 556 | Immunoglobulin M deficiency | 2 | Human disease | 9.0 |
| 564 | Difference of sexual development, generic | 24 | Human disease | 15.0 |
| 565 | Intestinal cobalamin malabsorption, AMN-related | 1 | Target evidence | 54.3 |
| 573 | Ciliary dyskinesia, primary, generic | 3 | Human gene | 35.0 |
| 578 | Krabbe disease | 4 | Target evidence | 85.1 |
| 586 | Legg-Calvé-Perthes disease | 5 | Human disease | 20.0 |
| 588 | Lens luxation | 3 | Target evidence | 59.7 |
| 593 | Acrodermatitis enteropathica | 3 | Target evidence | 69.3 |
| 595 | Leukocyte adhesion deficiency, type I | 5 | Drug | 84.0 |
| 615 | Lymphosarcoma | 3 | Human disease | 12.5 |
| 616 | Lysosomal storage disease | 6 | Human disease | 32.5 |
| 618 | Macrostomus | 2 | Human disease | 12.0 |
| 620 | Histiocytosis, malignant | 8 | Human gene | 32.5 |
| 621 | Malignant hyperthermia | 8 | Human gene | 35.0 |
| 625 | Mannosidosis, alpha | 7 | Target evidence | 95.0 |
| 626 | Mannosidosis, beta | 5 | Target evidence | 63.9 |
| 627 | Maple syrup urine disease, BCKDHA-related | 1 | Target evidence | 63.4 |
| 628 | Marfan syndrome, FBN1-related | 4 | Target evidence | 88.0 |
| 629 | Megacolon | 5 | Drug | 64.7 |
| 633 | Melanoma, Sinclair swine cutaneous malignant | 1 | Human disease | 9.0 |
| 636 | Membranoproliferative glomerulonephritis type II | 1 | Human gene | 29.0 |
| 640 | Menkes disease | 2 | Target evidence | 88.9 |
| 642 | Mesangiocapillary glomerulonephritis, type I | 1 | Human disease | 9.0 |
| 645 | Microcephaly | 1 | Human disease | 6.5 |
| 648 | Micromelia | 3 | Human disease | 15.0 |
| 649 | Microphthalmia | 11 | Target evidence | 35.3 |
| 653 | Mitral stenosis | 2 | Human disease | 29.5 |
| 654 | Myxomatous valvular degeneration | 8 | Human disease | 15.0 |
| 655 | Mitral valve stenosis | 1 | Human disease | 26.5 |