Comparative

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
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
366 Fanconi syndrome 4 Target evidence 63.7
369 Feather colour, oculocutaneous albinism type I (OCA1), TYR-related 6 Drug 61.4
370 Feather colour, SLC45A2-related 6 Target evidence 66.6
388 Fibrodysplasia ossificans 3 Drug 85.6
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
394 Frizzle, KRT6A-related 1 Human gene 21.0
396 Fucosidosis, alpha 2 Target evidence 61.2
400 Galactosialidosis 1 Human disease 9.0
402 Gangliosidosis, GM1 5 Target evidence 64.7
404 Gastric dilatation volvulus syndrome 4 Human disease 15.0
405 Gaucher disease, generic 3 Human disease 40.0
409 Gingival hypertrophy 2 Human disease 9.5
411 Glaucoma, generic 8 Human disease 15.0
413 Glomerulonephritis 2 Human disease 12.0
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
428 Haemochromatosis 10 Human disease 15.0
432 Haemolytic anaemia, autoimmune 2 Human disease 37.0
437 Haemophilia A 7 Drug 96.7
438 Haemophilia B 4 Drug 96.0
439 Hair, long 13 Human disease 14.0
444 Cleft lip 3 Human disease 12.5
446 Heart defect, congenital 10 Human disease 37.5
452 Henny feathering 1 Drug 53.6
453 Hepatic encephalopathy 3 Human disease 12.5
454 Hepatic fibrosis, idiopathic 2 Human disease 12.0
459 Hernia, diaphragmatic 10 Human disease 15.0
461 Hernia, hiatal 2 Human disease 12.0
462 Hernia, inguinal 6 Human disease 15.0
468 Heterochromia irides/iridis/iridum 5 Human disease 15.0
473 Hip dysplasia 11 Human disease 15.0
476 Hodgkin disease 1 Human disease 34.0
478 Holoprosencephaly 4 Human disease 15.0
483 Polled/Horns 8 Human gene 29.0
485 Huntington disease 4 Human disease 39.0
486 Hydranencephaly 3 Human disease 12.5
487 Hydrocephalus 12 Target evidence 63.9
493 Hydrops foetalis 5 Human disease 15.0
494 Cushing syndrome, generic 7 Human disease 15.0
495 Hyperbilirubinaemia, generic 5 Human disease 15.0
496 Hyperbilirubinaemia I 3 Human disease 12.0