Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "H"

141 to 150 of 426 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
141	3060	HCRT	Hypocretin neuropeptide precursor	NRCLP1, OX, PPOX	Amnesia, Cataplexy, Degenerative diseases, central nervous system, Hallucinations, Mental depression, Narcolepsy, Narcolepsy-cataplexy syndrome, Neurodegenerative disorders, Obesity, Paroxysmal drowsiness
142	3061	HCRTR1	Hypocretin receptor 1	ORXR1, OX1R, OXR1	Mental depression, Mood disorder, Schizophrenia
143	3062	HCRTR2	Hypocretin receptor 2	ORXR2, OX2R, OXR2	Narcolepsy, Narcolepsy-cataplexy syndrome
144	3064	HTT	Huntingtin	HD, IT15, LOMARS	Akinetic-rigid variant of huntington disease, Cerebellar ataxia, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Dementia, Developmental delay, Developmental regression, Dysphagia, Huntington disease, Mental retardation, Lopes-maciel-rodan syndrome, Mental depression, Mood disorder, Movement disorders, Myopia, Scoliosis, Status marmoratus View all (3 more)
145	3065	HDAC1	Histone deacetylase 1	GON-10, HD1, KDAC1, RPD3, RPD3L1	Carcinoma, Endometrioma, Endometriosis, Heart diseases, Mood disorder, Myelodysplastic syndrome, Pulmonary arterial hypertension, Pulmonary hypertension, Pulmonary hypertension with hereditary hemorrhagic telangiectasia, Schizophrenia
146	3066	HDAC2	Histone deacetylase 2	HD2, KDAC2, RPD3, YAF1	Carcinoma, Chronic obstructive pulmonary disease, Endometrioma, Endometriosis, Liver cirrhosis, Liver fibrosis, Melanoma, Mental depression, Monocytic leukemia, Mood disorder, Myeloid leukemia, Nonorganic psychosis, Prostate adenocarcinoma, Psychosis, Schizophrenia
147	3067	HDC	Histidine decarboxylase	-	Attention deficit hyperactivity disorder, Colorectal cancer, Dyssomnia, Obsessive-compulsive disorder, Sleep disorders, Tourette syndrome
148	3069	HDLBP	High density lipoprotein binding protein	HBP, PRO2900, VGL	2q37 deletion syndrome, Autism, Breast cancer, Lymphocytic leukemia
149	3070	HELLS	Helicase, lymphoid specific	ICF4, LSH, Nbla10143, PASG, SALNR, SMARCA6	Agammaglobulinemia, Anemia, Communicating hydrocephalus, Congenital epicanthus, Congenital exomphalos, Developmental delay, Dwarfism, Immunodeficiency-centromeric instability-facial anomalies syndrome, Immunodeficiency, Lung adenocarcinoma, Lymphopenia, Macrocephaly, Macroglossia, Malabsorption syndrome, Mental retardation View all (4 more)
150	3073	HEXA	Hexosaminidase subunit alpha	TSD	Amaurotic idiocy, Dementia, Developmental regression, Gangliosidosis, Hexosaminidase a deficiency, Mental retardation, Movement disorders, Pseudodeficiency of beta-hexosaminidase a, Subacute gangliosidosis, Tay-sachs disease

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