Genes | GeDiPNet - Gene Disease Pathway & Associations

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8481 to 8490 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
8481	8923210	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)
8482	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
8483	6775063	ND6	-	-	Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy
8484	8923198	ND6	-	-	Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy
8485	55706	NDC1	NDC1 transmembrane nucleoporin	NET3, TMEM48	Global developmental delay, Major depressive disorder, Mood disorder, Neurodevelopmental disorder, Polyneuropathy, Uranostaphyloschisis
8486	10403	NDC80	NDC80 kinetochore complex component	HEC, HEC1, HsHec1, KNTC2, TID3, hsNDC80	Hepatocellular carcinoma
8487	54820	NDE1	NudE neurodevelopment protein 1	HOM-TES-87, LIS4, MHAC, NDE, NUDE, NUDE1	Aortic aneurysm, Intestinal pseudo-obstruction, Congenital aneurysm of ascending aorta, Connective tissue disease, Thoracic aortic aneurysm and aortic dissection, Hydranencephaly, Intellectual developmental disorder, Left ventricular disease, Lissencephaly, Macrogyria, Megacystis microcolon intestinal hypoperistalsis syndrome, Microcephaly, Microhydranencephaly, Microlissencephaly, Myopia View all (7 more)
8488	81565	NDEL1	NudE neurodevelopment protein 1 like 1	EOPA, MITAP1, NDE1L1, NDE2, NUDEL	Juvenile arthritis, Color vision deficiency, Juvenile idiopathic arthritis, Non-organic psychosis, Oligoarticular juvenile idiopathic arthritis, Psoriasis, Psychotic disorders, Schizophrenia
8489	80762	NDFIP1	Nedd4 family interacting protein 1	N4WBP5	Ankylosing spondylitis, Asthma, Eczema, Biliary cirrhosis, Breast cancer, Cancer, Corneal astigmatism, Crohn disease, Dementia, Inflammatory bowel disease, Multiple sclerosis, Biliary cholangitis, Psoriasis, Respiratory system disease, Sclerosing cholangitis View all (4 more)
8490	54602	NDFIP2	Nedd4 family interacting protein 2	N4WBP5A	Major depressive disorder

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