Comparative

Disease groups

2,194 disease groups, by OMIA group number.

OMIA group Name Species The chain reached Best score
2565 Amastia, congenital 2 Human disease 12.0
2567 Gallbladder, agenesis of 1 Human disease 9.0
2568 Endometritis, predisposition to 4 Animal disease only
2570 Chlamydia infection, susceptibility/resistance to 1 Animal disease only
2571 5-Hydroxytryptamine deficiency 1 Animal disease only
2573 Lewy body-like disease, CADPS2-related 1 Animal disease only
2574 Corneal sequestra 1 Animal disease only
2575 Alzheimer, SORL1-related 1 Animal disease only
2576 Osseous choristoma of the ciliary body 1 Animal disease only
2577 Lethality, RYR2-related 1 Animal disease only
2578 Mast cell tumour, congenital 1 Animal disease only
2579 Perinatal mortality syndrome, GCK-related 1 Animal disease only
2580 Night blindness 2 Human disease 34.5
2581 Pelvic organ prolapse, predisposition to 6 Human disease 15.0
2582 Hepatocellular fibrinogen storage disease 1 Human gene 26.5
2583 Dental abnormalities 7 Animal disease only
2584 Deafness, CDH23-related 1 Human gene 29.0
2585 Acyl-CoA dehydrogenase, medium chain, deficiency of 1 Target evidence 78.9
2586 Lymphoma, B-cell, predisposition to 4 Animal disease only
2587 Neoplasm, generic 31 Animal disease only
2588 Cardiomyopathy, arrhythmogenic left ventricular 1 Animal disease only
2590 Cleft palate, MYH3-related 1 Animal disease only
2591 Lysosomal storage disease, CNP-related 1 Animal disease only
2592 Theileriosis, susceptibility/resistance to 2 Animal disease only
2596 Dwarfism, ANKRD28-related 1 Animal disease only
2597 Haplotypes with homozygous deficiency HH18-HH38 1 Animal disease only
2599 Iris sphincter dysplasia 1 Animal disease only
2600 Amelogenesis imperfecta, FAM83H-related 1 Human disease 10.0
2602 Cerebellar abiotrophy, VMP1-related 1 Animal disease only
2606 Skeletal dysplasia 3, PCYT1A-related 1 Target evidence 57.2
2607 Pyknodysostosis 1 Human disease 9.0
2610 Dacryocystitis 1 Human disease 6.5
2611 Muscular dystrophy, limb-girdle, CAPN3-related 1 Human disease 10.0
2614 Angelman syndrome 1 Human disease 25.0
2615 Testicular agenesis 1 Human disease 6.5
2616 Neuropathy, hereditary sensory and autonomic, SCN9A-related 1 Human disease 14.0
2618 Nephropathy, COL4A4 related 1 Drug 64.9
2619 Hypogonadotropic hypogonadism, KISS1-related 1 Human disease 10.0
2621 Gaucher disease, type II 1 Drug 64.7
2623 Ciliary dyskinesia, primary, STK36-related 1 Target evidence 53.7
2624 Usher syndrome, USH2A-related 1 Human disease 10.0
2625 Skeletal dysplasia, FGD3-related 1 Animal disease only
2626 Haplotype with homozygous deficiency JBH17, CDC45-related 1 Human gene 29.0
2631 Delayed postoperative hemorrhage 1 Target evidence 52.3
2632 Asthenoteratozoospermia, SSX1-related 2 Human disease 5.0
2634 Meningioma 3 Human disease 15.0
2636 Anterior segment dysgenesis 3 Human disease 15.0
2637 Adaptation, environment, generic 86 Animal disease only
2640 Epizootic haemorrhagic disease, susceptibility/resistance to 1 Animal disease only
2641 Thoracolumbar myelopathy 1 Animal disease only