Comparative

Disease groups

2,194 disease groups, by OMIA group number.

OMIA group Name Species The chain reached Best score
2809 Trichiasis, caruncular 1 Animal disease only
2810 Neonatal diarrhoea, Escherichia coli F17, susceptibility/resistance to 1 Animal disease only
2811 Multiple ocular defects, COL11A1-related 1 Drug 65.2
2814 Polioencephalopathy, MECR-related 1 Target evidence 57.1
2815 NPY2R deficiency 1 Animal disease only
2816 Mastocytosis, cutaneous 1 Human disease 29.0
2819 Muscle weakness, CACNA1S-related 1 Drug 58.3
2820 DND1 deficiency 1 Animal disease only
2821 Heart defect with mitral regurgitation 1 Animal disease only
2822 Uterine aplasia 6 Animal disease only
2824 Tricuspid valve atresia 1 Human disease 14.0
2825 Dichelobacter nodosus / Fusobacterium necrophorum infection, susceptibility/resistance to 1 Animal disease only
2828 Neospora caninum infection, susceptibility/resistance to 1 Animal disease only
2829 Circovirus infection, susceptibility/resistance to 1 Animal disease only
2830 Hyperuricaemia 2 Animal disease only
2832 Lethality, embryonic, POU5F1-related 1 Animal disease only
2834 Spondyloepiphyseal dysplasia tarda 1 Human disease 9.0
2835 Immunodeficiency, CARMIL2-related 1 Target evidence 56.3
2836 Babesiosis, susceptibility/resistance to 2 Animal disease only
2838 Pontocerebellar hypoplasia, AMPD2-related 1 Target evidence 62.4
2839 Muscle hypertrophy, dysphagia, and gait abnormalities 1 Animal disease only
2840 Leigh syndrome, NDUFS7-related 1 Drug 68.2
2842 Steroid-responsive meningitis-arteritis, predisposition to 1 Animal disease only
2846 Spinocerebellar ataxia, juvenile, FDXR-related 1 Target evidence 54.5
2847 Microphthalmia with haematopoietic defects, DNAJC21-related 1 Human gene 29.0
2848 Spermatogenic failure, QRICH2-related 1 Target evidence 36.7
2849 Methylmalonic-coA mutase deficiency 1 Target evidence 57.9
2850 Haplotype with homozygous deficiency, MTRDHH2 to 5 1 Animal disease only
2851 PDCD1-deficiency 1 Human disease 5.0
2852 Nasolacrimal duct obstruction 6 Human disease 15.0
2853 Sea louse, susceptibility/resistance to 1 Animal disease only
2854 Immunodeficiency, CARD9-related 1 Animal disease only
2855 Hypoxanthine guanine phosphoribosyltransferase deficiency 1 Human disease 25.0
2857 Myelopathy, hereditary 1 Animal disease only
2858 Methaemoglobinaemia, CYB5A-related 1 Human gene 21.0
2860 MIR137-deficiency 1 Animal disease only
2861 Psoroptic mange, susceptibility/resistance to 1 Animal disease only
2862 Haplotype with homozygous deficiency, SLC33A1-related 1 Target evidence 54.3
2864 Cardiomyopathy, left ventricular noncompaction 2 Human disease 12.0
2865 Cerebral palsy, RHOB-related 1 Animal disease only
2866 Corpus callosum hypoplasia / dysplasia 2 Animal disease only
2867 Encephalopathy, generic 1 Animal disease only
2868 Dyskinesia, paroxysmal, PCK2-related 1 Animal disease only
2869 Fibroblast growth factor 10 deficiency 1 Animal disease only
2870 Myelodysplastic syndrome 2 Human disease 42.0
2872 Lymphocyte intestinal retention defect 1 Animal disease only
2873 Haplotype with homozygous deficiency, RFC5-related 1 Animal disease only
2874 Haplotype with homozygous deficiency, NOA1-related 1 Animal disease only
2876 Neuroaxonal dystrophy, RNF170-related 1 Target evidence 59.2
2878 Diabetes mellitus, HNF1A-related 1 Human disease 10.0