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 |
|---|---|---|---|---|
| 664 | Mucopolysaccharidosis I | 4 | Target evidence | 84.7 |
| 665 | Mucopolysaccharidosis IIID | 1 | Target evidence | 62.3 |
| 666 | Mucopolysaccharidosis VI | 2 | Target evidence | 87.5 |
| 667 | Mucopolysaccharidosis VII | 2 | Target evidence | 92.8 |
| 679 | Muscular dystrophy | 7 | Target evidence | 58.0 |
| 683 | Muscular hypertrophy (double muscling) | 16 | Drug | 54.1 |
| 684 | Myasthenia | 4 | Human disease | 40.0 |
| 685 | Myasthenic syndrome, congenital, CHRNE-related | 3 | Human gene | 35.0 |
| 689 | Hyperekplexia, GLRA1-related | 3 | Human gene | 40.0 |
| 690 | Myoclonus epilepsy of Lafora | 5 | Target evidence | 61.8 |
| 693 | Myopathy | 5 | Human disease | 37.5 |
| 694 | Myopathy, congenital | 2 | Human disease | 14.5 |
| 695 | Myopathy, mitochondrial | 1 | Human disease | 26.5 |
| 697 | Myositis ossificans | 2 | Human disease | 9.5 |
| 698 | Myotonia | 8 | Target evidence | 81.1 |
| 699 | Myotonic dystrophy | 1 | Human disease | 29.0 |
| 702 | Nanomelia | 1 | Target evidence | 55.3 |
| 703 | Narcolepsy | 4 | Human gene | 35.0 |
| 706 | Necrotising myelopathy, IBA57-related | 1 | Target evidence | 56.7 |
| 708 | Nephritis | 1 | Human disease | 26.5 |
| 709 | Nephrolithiasis | 3 | Human disease | 37.5 |
| 712 | Nephrotic syndrome | 2 | Human disease | 12.0 |
| 716 | Neurofibromatosis, generic | 3 | Target evidence | 90.9 |
| 725 | Niemann-Pick disease, type C1 | 3 | Target evidence | 88.1 |
| 729 | Teat / nipple, inverted | 2 | Human disease | 12.0 |
| 731 | Nystagmus, congenital | 1 | Human disease | 21.5 |
| 735 | Ocular squamous cell carcinoma | 6 | Human disease | 15.0 |
| 740 | Olivopontocerebellar atrophy | 1 | Human disease | 29.0 |
| 741 | Omphalocele | 4 | Human disease | 15.0 |
| 743 | Optic nerve hypoplasia, bilateral | 1 | Human disease | 9.0 |
| 745 | Orchitis | 2 | Human disease | 34.5 |
| 747 | Osteoarthritis | 8 | Human disease | 15.0 |
| 748 | Osteochondritis dissecans | 3 | Human disease | 12.5 |
| 750 | Osteochondrosis | 11 | Human disease | 15.0 |
| 753 | Osteodystrophy | 4 | Human disease | 30.0 |
| 754 | Osteogenesis imperfecta, generic | 4 | Human disease | 15.0 |
| 755 | Osteopetrosis | 7 | Target evidence | 37.0 |
| 765 | Pancreatic insufficiency, exocrine | 3 | Human disease | 37.5 |
| 770 | Tremor, X-linked, PLP1-related | 4 | Target evidence | 69.9 |
| 779 | Patent ductus arteriosus | 7 | Human disease | 15.0 |
| 781 | Patent urachus | 7 | Human disease | 12.5 |
| 783 | Pelger-Huet anomaly | 3 | Human disease | 15.0 |
| 785 | Hyperkalemic Periodic Paralysis, HYPP | 1 | Drug | 78.5 |
| 786 | Peromelia | 2 | Human disease | 12.0 |
| 791 | Persistent Mullerian duct syndrome, generic | 3 | Human disease | 20.0 |
| 795 | Persistent truncus arteriosus | 7 | Human disease | 12.5 |
| 801 | Pityriasis rosea | 1 | Human disease | 6.5 |
| 804 | Pneumothorax | 2 | Human disease | 32.0 |
| 805 | Polyarthritis | 2 | Human disease | 9.5 |
| 807 | Polycystic kidney disease | 14 | Human gene | 40.0 |