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Refine by Category Mitochondrial complex I deficiency 8 Leber hereditary optic neuropathy 6 Leigh syndrome 5 Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome 4 2,4-dienoyl-CoA reductase deficiency 2 Alzheimer disease mitochondrial 2 Leber hereditary optic neuropathy with dystonia 2 D-bifunctional protein deficiency 1 Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency 1 Methylmalonate semialdehyde dehydrogenase deficiency 1 Deafness, autosomal dominant, 40 1 Hyperprolinemia 2 1 Microcephaly, congenital cataract, and psoriasiform dermatitis 1 Deafness, X-linked, 5 1 Hypertriglyceridemia, transient infantile 1 Microphthalmia, isolated, 8 1 3-alpha-hydroxyacyl-CoA dehydrogenase deficiency 1 Diabetes mellitus, non-insulin-dependent 1 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1 1 Adrenal hyperplasia 2 1
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