5781
|
|
|
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 |
5782
|
|
|
Hes related family bHLH transcription factor with YRPW motif like |
HESR3, HEY3, HRT3, bHLHb33 |
|
5783
|
|
|
Homeostatic iron regulator |
HFE1, HH, HLA-H, MVCD7, TFQTL2 |
Alzheimer disease, Anemia, 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, Hematologic disease, Hemochromatosis, Hepatic veno occlusive disease, Hereditary hemochromatosis, Hypertension, Intestinal obstruction, Iron metabolism disorder, Juvenile idiopathic arthritis, Liver cirrhosis, Liver disease, Major depressive disorder, Metabolic syndrome, Myelodysplastic syndrome, Myocardial infarction, Neurotic disorder, Nonalcoholic fatty liver disease, Obesity, Obsessive-compulsive disorder, Osteoarthritis, Iron deficiency anemia, Parkinson disease, Oligoarticular juvenile idiopathic arthritis, Peripheral neuropathy, Polycythemia, Polymyalgia rheumatica, Porphyria cutanea tarda, Porphyruria, Respiratory system disease, Rheumatoid arthritis, Schizophrenia, Variegate porphyriaView all (30 more) |
5784
|
|
|
Helicase for meiosis 1 |
MER3, POF9, SEC63D1, Si-11, Si-11-6, helicase |
|
5785
|
|
|
Homogentisate 1,2-dioxygenase |
AKU, HGO |
|
5786
|
|
|
Hepatocyte growth factor |
DFNB39, F-TCF, HGFB, HPTA, SF |
Angle closure glaucoma, Astrocytoma, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Barrett esophagus, Hepatocellular carcinoma, Squamous cell carcinoma, Cardiomyopathy, Copper overload cirrhosis, Deafness, Diabetic neuropathy, Gout, Graft-versus-host disease, Hearing impairment, Hearing loss, Hereditary hearing loss, Hyperbilirubinemia, Hypertension, Keratoconus, Myeloid leukemia, Liver cirrhosis, Liver failure, Liver neoplasms, Lung disease, Mesothelioma, Multiple myeloma, Myocardial infarction, Myocardial ischemia, Myopia, Neuroblastoma, Oligodendroglioma, Pancreatitis, Parkinson disease, Prostate cancer, Pulmonary fibrosis, Systemic sclerosis, Thrombosis, Vascular disease, VitiligoView all (25 more) |
5787
|
|
|
HGF activator |
HGFA |
Hepatocellular carcinoma, Cardiovascular disease, Coronary artery disease, Crohn disease, Hyperlipidemia, Gallstones, Inflammatory bowel disease, Insomnia, Metabolic syndrome, Diabetes mellitus type 2, Ulcerative colitis, Venous thromboembolism |
5788
|
|
|
HGH1 cochaperone |
BRP16, BRP16L, C8orf30A, C8orf30B, FAM203A, FAM203B |
|
5789
|
|
|
Heparan-alpha-glucosaminide N-acetyltransferase |
HGNAT, MPS3C, RP73, TMEM76 |
|
5790
|
|
|
Hedgehog acyltransferase |
MART2, NNMS, SKI1, Skn |
Ankylosing spondylitis, Cardiovascular disease, Chondrodysplasia-difference of sex development syndrome, Chondrodysplasia-pseudohypohermaphroditism syndrome, Coronary artery disease, Gastrointestinal stromal tumor, Hyperopia, Large artery stroke, Nervous system disease, Schizophrenia, Stroke |
