Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "H"

181 to 190 of 495 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
181	8820	HESX1	HESX homeobox 1	ANF, CPHD5, RPX	Alzheimer disease, Anophthalmia/microphthalmia-esophageal atresia syndrome, Combined pituitary hormone deficiency, Desbuquois syndrome, Growth hormone deficiency with pituitary anomalies, Hypothyroidism, Kallmann syndrome, Male infertility spermatogenesis disorder, Panhypopituitarism, Pituitary hormone deficiency, Pituitary stalk interruption syndrome, Septo-optic dysplasia
182	3073	HEXA	Hexosaminidase subunit alpha	TSD	Beta-hexosaminidase a deficiency, Global developmental delay, Gm2 gangliosidosis, Hearing impairment, Intellectual developmental disorder, Leukodystrophy, Tay-sachs disease
183	3074	HEXB	Hexosaminidase subunit beta	ENC-1AS, HEL-248, HEL-S-111	Kidney failure, Sandhoff disease, Spinal muscular atrophy
184	284004	HEXD	Hexosaminidase D	HEXDC	Colorectal adenoma, Colorectal cancer
185	10614	HEXIM1	HEXIM P-TEFb complex subunit 1	CLP1, EDG1, HIS1, MAQ1	Asthma, Insomnia, Liver cirrhosis, Osteoarthritis
186	124790	HEXIM2	HEXIM P-TEFb complex subunit 2	L3	Androgenetic alopecia, Insomnia
187	23462	HEY1	Hes related family bHLH transcription factor with YRPW motif 1	BHLHb31, CHF2, HERP2, HESR1, HRT-1, NERP2, OAF1, hHRT1	Astrocytoma, Autism, Breast neoplasms, Pancreatic ductal carcinoma, Congenital heart disease, Glioblastoma, Lung neoplasms, Oligodendroglioma, Urethral obstruction
188	23493	HEY2	Hes related family bHLH transcription factor with YRPW motif 2	CHF1, GRIDLOCK, GRL, HERP1, HESR2, HRT2, bHLHb32	Astrocytoma, Breast neoplasms, Brugada syndrome, Pancreatic ductal carcinoma, Cardiomyopathy, Congenital heart disease, Thoracic aortic aneurysm and aortic dissection, Hypertrophic cardiomyopathy, Marfan syndrome, Metabolic syndrome, Migraine, Tetralogy of fallot, Diabetes mellitus type 2, Urethral obstruction
189	26508	HEYL	Hes related family bHLH transcription factor with YRPW motif like	HESR3, HEY3, HRT3, bHLHb33	Alzheimer disease, Breast neoplasms, Obstructive pulmonary disease, Hypertension, Irritable bowel syndrome, Metabolic syndrome, Migraine, Myocardial infarction, Diabetes mellitus type 2
190	3077	HFE	Homeostatic iron regulator	HFE1, HH, HLA-H, MVCD7, TFQTL2	Alzheimer disease, Anemia, Aphthous stomatitis, Autism, Beta thalassemia, Cardiomyopathy, Dilated cardiomyopathy, Cardiovascular disease, Congenital neurologic anomalies, Crohn disease, Cystic fibrosis, Diabetes mellitus, Diabetes mellitus type 2, Diabetic retinopathy, Digenic hemochromatosis View all (32 more)

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