|
141
|
|
|
Glutaryl-CoA dehydrogenase |
ACAD5, GCD |
Choreoathetosis, Developmental delay, Developmental regression, Dyskinetic syndrome, Epileptic encephalopathy, Glutaryl-coa dehydrogenase deficiency, Hypoglycemia, Impaired cognition, Ketonuria, Spastic diplegia, Macrocephaly, Migraine, Peripheral demyelination, Speech disorders |
|
142
|
|
|
Glucagon |
GLP-1, GLP1, GLP2, GRPP |
Anorexia, Catalepsy, Colitis, Colonic neoplasms, Compensatory hyperinsulinemia, Congestive heart failure, Diabetes mellitus, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Heart diseases, Heart failure, Hyperglycemia, Hyperinsulinism, Hyperlipidemia, Hypertension, Myocardial infarction, Obesity, Sinus tachycardia, Stomach diseases, Vascular diseasesView all (5 more) |
|
143
|
|
|
Glucagon receptor |
GGR, GL-R, MVAH |
|
|
144
|
|
|
GTP cyclohydrolase 1 |
DYT14, DYT5, DYT5a, GCH, GTP-CH-1, GTPCH1, HPABH4B |
6-pyruvoyl-tetrahydropterin synthase deficiency, Anxiety disorder, Choreoathetosis, Congenital clubfoot, Developmental delay, Dyskinesia, Dysphagia, Dyssomnia, Dystonia, dopa-responsive, with or without hyperphenylalaninemia, Gtp cyclohydrolase i deficiency, Horizontal nystagmus, Hyperphenylalaninemia, Hypertension, Hypothyroidism, Mental depression, Myocardial ischemia, Nonorganic psychosis, Obsessive-compulsive disorder, Parkinson disease, Psychosis, Rheumatoid arthritis, Schizophrenia, Scoliosis, Sleep disorders, Spastic paraplegia, Transient hyperphenylalaninemia, Writer`s crampView all (12 more) |
|
145
|
|
|
Glucokinase |
FGQTL3, GK, GLK, HHF3, HK4, HKIV, HXKP, LGLK, MODY2, PNDM1 |
Apraxia, Arthrogryposis multiplex congenita, Clinodactyly, Congenital heart defects, Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Coronary artery disease, Developmental delay, Diabetes mellitus, Exocrine pancreatic insufficiency, Hepatocellular adenoma, Hyperglycemia, Hyperinsulinism, Hypoglycemic coma, Hypoglycemic seizures, Hypoinsulinemia, Mental retardation, Ketonuria, Ketosis, Kidney disease, Mason type diabetes, Metabolic syndrome, Monogenic diabetes, Motor delay, Myoclonic seizures, Hypoglycemia, Nervous system diseases, Obesity, Peripheral axonal neuropathy, Ptosis, Renal cyst, Renal tubular disorder, Retinal diseases, SeizureView all (19 more) |
|
146
|
|
|
Glucokinase regulator |
FGQTL5, GKRP |
Ankylosing spondylitis, Atrial fibrillation, Cardiovascular diseases, Cholangitis, Coronary heart disease, Crohn disease, Diabetes, Diabetes mellitus, Gout, Gouty arthritis, Heart failure, Inflammatory bowel disease, Kidney disease, Kidney failure, Malignant neoplasm, Metabolic syndrome, Non-alcoholic fatty liver disease, Psoriasis, Stroke, Ulcerative colitis, UrolithiasisView all (6 more) |
|
147
|
|
|
Glucosaminyl (N-acetyl) transferase 1 |
C2GNT, C2GNT-L, C2GNT1, C2GlcNAcT, G6NT, NACGT2, NAGCT2 |
|
|
148
|
|
|
Glucosaminyl (N-acetyl) transferase 2 (I blood group) |
CCAT, CTRCT13, GCNT2C, GCNT5, IGNT, II, NACGT1, NAGCT1, ULG3, bA360O19.2, bA421M1.1 |
|
|
149
|
|
|
Glycine cleavage system protein H |
GCE, MMDS7, NKH |
|
|
150
|
|
|
Growth differentiation factor 1 |
CERS1, CHTD6, DORV, DTGA3, LAG1, LASS1, RAI, UOG1 |
Agenesis of corpus callosum, Aortic coarctation, Asplenia, Atrial isomerism, Atrial septal defect, Atrioventricular septal defect, Brachydactyly, Camptodactyly of fingers, Ciliopathies, Complete atrioventricular canal defect, Congenital atresia of pulmonary artery, Congenital heart defects, Conotruncal heart defect, Cryptorchidism, Dolichocephaly, Double outlet right ventricle, Heterotaxia, Left atrial isomerism, Myoclonic epilepsy, Patent foramen ovale, Polysplenia, Proptosis, Pulmonary stenosis, Pulmonary venous return anomaly, Right aortic arch, Right sided atrial isomerism, Secundum atrial septal defect, Single ventricle defect, Situs ambiguus, Taussig-bing anomaly, Tetralogy of fallot, Transposition of great vessels, Ventricular septal defectView all (18 more) |
