|
201
|
|
|
3-hydroxy-3-methylglutaryl-CoA lyase |
HL, HMGCL1 |
Anemia, Anorexia, Cardiomyopathy, Deficiency of hydroxymethylglutaryl-coa lyase, Dysarthria, Epileptic encephalopathy, Hemiplegia, Hmg coa lyase deficiency, Hyperuricemia, Hypoglycemia, Hypoglycemic coma, Mental retardation, Ketonuria, Leukoencephalopathy, Leukopenia, Microcephaly, Pancreatitis, ThrombocytosisView all (3 more) |
|
202
|
|
|
3-hydroxy-3-methylglutaryl-CoA reductase |
LDLCQ3, LGMDR28, MYPLG |
Autoimmune diseases, Carcinoma, Cardiovascular diseases, Coronary heart disease, Deficiency of mevalonate kinase, Hypercholesterolemia, Hyperimmunoglobulinemia, Hyperlipoproteinemia, Kidney failure, Liver carcinoma, Myopathy, Q fever |
|
203
|
|
|
3-hydroxy-3-methylglutaryl-CoA synthase 2 |
- |
|
|
204
|
|
|
High mobility group AT-hook 1 |
HMG-R, HMGA1A, HMGIY |
|
|
205
|
|
|
Hyaluronan mediated motility receptor |
CD168, IHABP, RHAMM |
|
|
206
|
|
|
Heme oxygenase 1 |
HMOX1D, HO-1, HSP32, bK286B10 |
Adrenoleukodystrophy, Adrenomyeloneuropathy, Alveolitis, Alzheimer disease, Amyloidosis, Anemia, Asthma, Blood coagulation disorders, Breast cancer, Mammary neoplasms, Breast carcinoma, Carotid artery disease, Carotid atherosclerosis, Chronic obstructive pulmonary disease, Cirrhosis, Colitis, Compensatory hyperinsulinemia, Congestive heart failure, Coronary arteriosclerosis, Coronary artery disease, Degenerative diseases, central nervous system, Dermatitis, Diabetes mellitus, Diabetic cardiomyopathy, Emphysema, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Gastric cancer, Gastroparesis, Grand mal status epilepticus, Heart failure, Heme oxygenase 1 deficiency, Hepatorenal syndrome, Hyperinsulinism, Hypertension, Indolent systemic mastocytosis, Intravascular hemolysis, Iron metabolism disorders, Kidney failure, Learning disorders, Liver neoplasms, Liver cancer, Lung neoplasms, Lung cancer, Marfan syndrome, Mastocytosis, Microangiopathic hemolytic anemia, Moyamoya disease, Myocardial infarction, Myocardial ischemia, Neurodegenerative disorders, Nonconvulsive status epilepticus, Obesity, Panacinar emphysema, Pancreatic diseases, Parkinson disease, Petit mal status, Prostatic neoplasms, Prostate cancer, Pulmonary emphysema, Pulmonary fibrosis, Acute kidney insufficiency, Retinal diseases, Schizophrenia, Senile dementia, Spinocerebellar ataxia, Status epilepticus, Stomach neoplasms, Systemic mastocytosisView all (54 more) |
|
207
|
|
|
H6 family homeobox 1 |
H6, NKX5-3 |
Cataract, Congenital ocular coloboma, Microcornea, Microphakia, Microphthalmos, Microtia, Nystagmus, Ocular hypertension, Oculoauricular syndrome, Rod-cone dystrophy, Sclerocornea |
|
208
|
|
|
Hepatocyte nuclear factor 4 alpha |
FRTS4, HNF4, HNF4a7, HNF4a8, HNF4a9, HNF4alpha, MODY, MODY1, NR2A1, NR2A21, TCF, TCF-14, TCF14 |
Arthritis, Absent vas deferens, Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Coronary heart disease, Developmental delay, Diabetes mellitus, Dwarfism, Dysmorphic features, Exocrine pancreatic insufficiency, Fanconi renotubular syndrome with maturity-onset diabetes of the young, Fanconi syndrome, Fatty liver, Hepatocellular adenoma, Horseshoe kidney, Hyperglycemia, Hyperinsulinism, Hyperuricemia, Hypoglycemia, Hypoinsulinemia, Hypophosphatemic rickets, Hypospadias, Hypothyroidism, Kidney disease, Malocclusion, Mason type diabetes, Mental retardation, Monogenic diabetes, Multicystic renal dysplasia, Hypotonia, Nephrocalcinosis, Obesity, Papillary cystadenoma of the epididymis, Phosphate diabetes, Renal agenesis, Renal carcinoma, Renal cyst, Renal cysts and diabetes syndrome, Renal glomerular disease, Retinal diseases, Rickets, Tubulointerstitial kidney disease, Ulcerative colitisView all (28 more) |
|
209
|
|
|
Hepatocyte nuclear factor 4 gamma |
NR2A2, NR2A3 |
|
|
210
|
|
|
Histamine N-methyltransferase |
HMT, HNMT-S1, HNMT-S2, MRT51 |
Absence of septum pellucidum, Asthma, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Rhinitis, Salaam seizures, Seizure, Sleep disorders, Stereotyped behavior, UrticariaView all (7 more) |
