Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

191 to 200 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
191	4537	ND3	Mitochondrially encoded NADH dehydrogenase 3	MTND3	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy in association with hereditary ataxia, Parkinson disease, Retinitis pigmentosa, Postaxial polydactyly
192	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 with hearing impairment, Optic atrophy, Optic neuritis View all (7 more)
193	4539	ND4L	Mitochondrially encoded NADH 4L dehydrogenase	MTND4L	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Diabetes mellitus, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, congenital hypomyelinating, Leber hereditary optic neuropathy, Retinitis pigmentosa, Postaxial polydactyly
194	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, congenital hypomyelinating, Parkinson disease, Retinitis pigmentosa, Postaxial polydactyly View all (1 more)
195	4541	ND6	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
196	4664	NAB1	NGFI-A binding protein 1	-	Eczema, Autoimmune disease, B-cell acute lymphoblastic leukemia, Biliary cirrhosis, Coronary artery disease, Crohn disease, Epilepsy, Generalized epilepsy, Hypertension, Inflammatory bowel disease, Multiple sclerosis, Myositis, Polymyositis, Biliary cholangitis, Rheumatoid arthritis View all (3 more)
197	4665	NAB2	NGFI-A binding protein 2	MADER	Attention deficit hyperactivity disorder, Insomnia, Schizophrenia
198	4666	NACA	Nascent polypeptide associated complex subunit alpha	HSD48, NAC-alpha, NACA1, skNAC	Atrial fibrillation, Cardiac arrhythmia, Pancreatic cancer
199	4668	NAGA	Alpha-N-acetylgalactosaminidase	D22S674, GALB	Alpha-n-acetylgalactosaminidase deficiency, Arthrogryposis multiplex congenita, Pena-shokeir syndrome type i, Schindler disease
200	4669	NAGLU	N-acetyl-alpha-glucosaminidase	CMT2V, MPS-IIIB, MPS3B, NAG, UFHSD	Asthma, Charcot-marie-tooth disease, Desbuquois syndrome, Hypertrichosis, Intellectual developmental disorder, Mucopolysaccharidosis, Parkinson disease, Prostatic neoplasm, Sanfilippo syndrome, Schizophrenia, Intellectual disability, Spastic ataxia, Diabetes mellitus, type 2

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