Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "H"

61 to 70 of 426 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
61	145864	HAPLN3	Hyaluronan and proteoglycan link protein 3	EXLD1, HsT19883	Colorectal neoplasms
62	148738	HJV	Hemojuvelin BMP co-receptor	HFE2, HFE2A, JH, RGMC	Arthritis, Arthropathy, Azoospermia, Cardiomyopathy, Cholestasis, Cirrhosis, Congenital hepatic fibrosis, Congestive heart failure, Coronary heart disease, Diabetes mellitus, Erectile dysfunction, Hemochromatosis, Hereditary hemochromatosis, Hypogonadism, Hypogonadotropic hypogonadism, Hypothyroidism, Osteoporosis View all (2 more)
63	150280	HORMAD2	HORMA domain containing 2	CT46.2	Breast carcinoma, Crohn disease, Diabetes mellitus, Glomerulonephritis, Hypothyroidism, Inflammatory bowel disease, Kidney disease, Lung cancer, Multiple sclerosis, Ulcerative colitis
64	164045	HFM1	Helicase for meiosis 1	MER3, POF9, SEC63D1, Si-11, Si-11-6, helicase	Ovarian failure, Premature menopause, Premature ovarian failure
65	170572	HTR3C	5-hydroxytryptamine receptor 3C	-	Autism, Colorectal cancer
66	1839	HBEGF	Heparin binding EGF like growth factor	DTR, DTS, DTSF, HEGFL	Arthritis, Atrial fibrillation, Cryptogenic tonic-clonic epilepsy, Endometrioma, Endometriosis, Epilepsy, Gastric cancer, Juvenile arthritis, Kidney failure, Left ventricular hypertrophy, Necrotizing enterocolitis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Acute kidney insufficiency, Still disease View all (2 more)
67	192286	HIGD2A	HIG1 hypoxia inducible domain family member 2A	HIG2A, RCF1b	Liver neoplasms, Liver cancer
68	200909	HTR3D	5-hydroxytryptamine receptor 3D	5HT3D	Schizophrenia
69	204851	HIPK1	Homeodomain interacting protein kinase 1	Myak, Nbak2	Ankylosing spondylitis, Cholangitis, Crohn disease, Gastrointestinal stromal tumor, Hypothyroidism, Psoriasis, Ulcerative colitis
70	219844	HYLS1	HYLS1 centriolar and ciliogenesis associated	HLS	Absence of septum pellucidum, Agenesis of corpus callosum, Arrhinencephaly, Atrioventricular septal defect, Cerebellar vermis agenesis, Ciliopathies, Agenesis of the diaphragm, Congenital atresia of trachea, Congenital cerebral hernia, Congenital coloboma of iris, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Hirschsprung disease View all (29 more)

«««...5 678 9...»»»