Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "N"
131 to 140 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

131
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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)

132
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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)

133
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

134
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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

135
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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

136
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
View all (1 more)

137
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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
View all (1 more)

138
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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
View all (1 more)

139
Mitochondrially encoded NADH dehydrogenase 6
MTND6
Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy

140
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Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy