Genes | GeDiPNet - Gene Disease Pathway & Associations

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8471 to 8480 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
8471	6775076	ND3	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly
8472	8923206	ND3	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly
8473	4538	ND4	Mitochondrially encoded NADH dehydrogenase 4	MTND4	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Dementia, Developmental delay, Epilepsy, Hearing impairment, Leber hereditary optic neuropathy, Macular degeneration, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Optic neuritis View all (7 more)
8474	6775072	ND4	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Dementia, Developmental delay, Epilepsy, Hearing impairment, Leber hereditary optic neuropathy, Macular degeneration, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Optic neuritis View all (7 more)
8475	8923197	ND4	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Dementia, Developmental delay, Epilepsy, Hearing impairment, Leber hereditary optic neuropathy, Macular degeneration, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Optic neuritis View all (7 more)
8476	4539	ND4L	Mitochondrially encoded NADH 4L dehydrogenase	MTND4L	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Diabetes mellitus, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Postaxial polydactyly
8477	6775071	ND4L	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Diabetes mellitus, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Postaxial polydactyly
8478	8923201	ND4L	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Diabetes mellitus, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Postaxial polydactyly
8479	4540	ND5	Mitochondrially encoded NADH dehydrogenase 5	MTND5	Hepatocellular carcinoma, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Developmental delay, Hearing impairment, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Myoclonic epilepsy with ragged red fibers, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly View all (1 more)
8480	6775066	ND5	-	-	Hepatocellular carcinoma, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Developmental delay, Hearing impairment, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Myoclonic epilepsy with ragged red fibers, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Parkinson disease, Rod-cone dystrophy, Postaxial polydactyly View all (1 more)

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