Comparative

Disease groups

2,194 disease groups, by OMIA group number.

OMIA group Name Species The chain reached Best score
1852 Haplotype with homozygous deficiency NH2 1 Animal disease only
1853 Haplotype with homozygous deficiency NH3 1 Animal disease only
1854 Haplotype with homozygous deficiency NH4 1 Animal disease only
1855 Haplotype with homozygous deficiency NH6 1 Animal disease only
1856 Tuberculosis, susceptibility/resistance to 6 Human disease 15.0
1857 Pentalogy of Fallot 4 Animal disease only
1858 Bone fracture risk 3 Animal disease only
1859 Horn cancer 1 Animal disease only
1860 Methane emissions 3 Animal disease only
1861 Chiari malformation Type I with syringomyelia 1 Human disease 9.0
1863 Medial coronoid disease 1 Animal disease only
1864 Ectodermal dysplasia/skin fragility syndrome, PKP1-related 1 Target evidence 60.9
1865 Cataract, diabetic 1 Human disease 9.0
1866 Hypotrichosis, Don Sphynx 1 Animal disease only
1867 Lissencephaly and cerebellar hypoplasia, RELN-related 2 Target evidence 64.5
1869 Retinal degeneration, Smoky Joe 1 Animal disease only
1870 Glaucoma, primary open angle, ADAMTS10-related 1 Human gene 29.0
1871 Glaucoma, primary closed-angle 1 Human disease 6.5
1872 Recurrent uveitis 1 Animal disease only
1874 Polymyositis 1 Human disease 9.0
1876 Retinal atrophy, progressive, SAG-related 1 Target evidence 52.4
1877 Pyoderma 1 Human disease 6.5
1878 Cystinuria, generic 2 Animal disease only
1879 Cystinuria, type II - A 1 Target evidence 83.6
1880 Cystinuria, type II - B 1 Target evidence 83.5
1881 Cystinuria, type III 1 Animal disease only
1882 Attention deficit hyperactivity disorder 1 Human disease 9.0
1883 Glycogen storage disease, generic 1 Animal disease only
1886 Chondrodysplasia, disproportionate short-limbed, ITGA10-related' 1 Animal disease only
1887 Osteopetrosis with gingival hamartomas 1 Target evidence 72.7
1888 Muscular dystrophy, Becker type 3 Drug 93.7
1891 Ectopic ureter 2 Animal disease only
1893 Upper airway syndrome 1 Animal disease only
1894 Cervical vertebral compressive myelopathy 4 Animal disease only
1896 Exercise-induced pulmonary haemorrhage 1 Animal disease only
1897 Hoof wall separation syndrome 1 Animal disease only
1898 Metabolic syndrome 2 Human disease 9.5
1899 Incontinentia pigmenti 1 Target evidence 63.1
1901 Haplotype with homozygous deficiency, RNASEH2B-related 1 Target evidence 55.8
1902 Male subfertility, TMEM95-related 1 Animal disease only
1903 Skeletal dysplasia with craniofacial deformity and disproportionate dwarfism 1 Animal disease only
1905 Johne's disease, susceptibility/resistance to 7 Animal disease only
1906 Haplotype with homozygous deficiency 05-826 1 Animal disease only
1907 Haplotype with homozygous deficiency 05-1351 and 05-1476 1 Animal disease only
1909 Haplotype with homozygous deficiency 07-501 1 Animal disease only
1910 Haplotype with homozygous deficiency 11-926, 11-976, 11-1001 and 11,1026 1 Animal disease only
1911 Haplotype with homozygous deficiency 19-151 1 Animal disease only
1913 Ataxia, cerebellar, juvenile to adolescent, RAB24-related 1 Animal disease only
1914 Peters anomaly 3 Human disease 15.0
1916 Familial adenomatous polyposis 3 Target evidence 66.4