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2811
|
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Endothelin 1 |
ARCND3, ET1, HDLCQ7, PPET1, QME |
Alveolitis, Asthma, Atrial fibrillation, Auriculocondylar syndrome, Cerebral infraction, Cardiomyopathy, Cardiovascular abnormalities, Cardiovascular diseases, Cartilage diseases, Cerebral thrombosis, Cerebrovascular disorders, Cerebrovascular insufficiency, Cerebrovascular occlusion, Chondromalacia, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital heart defects, Congestive heart failure, Coronary artery disease, Developmental delay, Diabetes mellitus, Erectile dysfunction, Functional gastrointestinal disorders, Gastrointestinal diseases, Glomerular hyalinosis, Glomerulosclerosis, Glossoptosis, Heart failure, Hepatorenal syndrome, Hypercholesterolemia, Hypertension, Involutional depression, Involutional paraphrenia, Kidney disease, Kidney failure, Laryngeal cleft, Left ventricular hypertrophy, Lewy body disease, Macrocephaly, Marginal ulcer, Mental depression, Microglossia, Micrognathism, Microstomia, Myocardial diseases, Myocardial infarction, Myocardial ischemia, Nephrosis, Oral ulcer, Parkinson disease, Paroxysmal atrial fibrillation, Peptic ulcer, Periauricular skin pits, Psychosis, Ptosis, Pulmonary fibrosis, Acute kidney insufficiency, Renal insufficiency, Respiratory distress syndrome, Sleep apnea, Stroke, Subarachnoid hemorrhage, Vein of galen aneurysmView all (49 more) |
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2812
|
|
|
Endothelin 3 |
ET-3, ET3, HSCR4, PPET3, WS4B |
Cardiovascular abnormalities, Colonic aganglionosis, Congenital central hypoventilation, Congenital intestinal aganglionosis, Dwarfism, Ganglioneuroblastoma, Ganglioneuroma, Haddad syndrome, Hearing loss, Hirschsprung disease, Hypertension, Impaired cognition, Intestinal obstruction, Intestinal polyposis, Lung diseases, Mental retardation, Mouth abnormalities, Ondine syndrome, Posteriorly rotated ear, Synophrys, Thyroid neoplasm, Waardenburg syndromeView all (7 more) |
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2813
|
|
|
Endothelin receptor type A |
ET-A, ETA, ETA-R, ETAR, ETRA, MFDA, hET-AR |
Alopecia, Breast cancer, Common migraine, Congenital heart defects, Congestive heart failure, Diabetes mellitus, Erectile dysfunction, Hearing loss, Heart failure, Hypertension, Hypoplasia of the maxilla, Mandibulofacial dysostosis, Mandibulofacial dysostosis with alopecia, Micrognathism, Microtia, Migraine with aura, Myocardial infarction, Narcolepsy, Nasopharyngeal neoplasms, Nasopharyngeal cancer, Ovarian neoplasm, Ovarian cancer, Sleep apnea, Stenosis of external auditory canal, Stroke, Trismus, Obstructive sleep apnea syndromeView all (12 more) |
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2814
|
|
|
Adenosylhomocysteinase |
SAHH, adoHcyase |
Antithrombin deficiency, Cardiomyopathy, Cerebellar hypoplasia, Developmental delay, Developmental regression, Disorder of amino acid metabolism, Esotropia, Fibrinogen deficiency, Glycine n-methyltransferase deficiency, Hepatic methionine adenosyltransferase deficiency, Hepatolenticular degeneration, Hydrops fetalis, Hypoalbuminemia, Hypofibrinogenemia, Hypoplasia of corpus callosum, Inherited errors of amino acid metabolism, Liver carcinoma, Lung adenocarcinoma, Mental retardation, Microcephaly, Motor delay, Muscular dystrophy, Non-alcoholic fatty liver disease, Respiratory failure, S-adenosylhomocysteine hydrolase deficiency, Sensorimotor neuropathyView all (11 more) |
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2815
|
|
|
Endothelin receptor type B |
ABCDS, ET-B, ET-BR, ETB, ETB1, ETBR, ETRB, HSCR, HSCR2, WS4A |
Abcd syndrome, Albinism, Anomalous pulmonary artery, Breast cancer, Mammary neoplasms, Breast carcinoma, Colonic aganglionosis, Congenital intestinal aganglionosis, Congestive heart failure, Developmental delay, Diabetes mellitus, Dwarfism, Hearing loss, Heart failure, Hirschsprung disease, Intestinal obstruction, Intestinal polyposis, Iron deficiency anemia, Leukodystrophy, Malnutrition, Marfan syndrome, Mental retardation, Multicystic renal dysplasia, Myocardial infarction, Nephrosis, Nystagmus, Polyneuropathy, Ptosis, Subarachnoid hemorrhage, Synophrys, Thyroid neoplasm, Total intestinal aganglionosis, Waardenburg syndromeView all (18 more) |
|
2816
|
|
|
Polyhomeotic homolog 1 |
EDR1, HPH1, MCPH11, RAE28 |
Agenesis of corpus callosum, Neoplasm, Developmental delay, Dwarfism, Embryonal neoplasm, Tumor, Mental retardation, Microcephaly, Neuronal heterotopia, Pachygyria, Renal aplasia, Vesicoureteral reflux |
|
2817
|
|
|
Eukaryotic translation elongation factor 1 alpha 1 |
CCS-3, CCS3, EE1A1, EEF-1, EEF1A, EF-Tu, EF1A, EF1A1, EF1alpha1, GRAF-1EF, LENG7, PTI1, eEF1A-1 |
|
|
2818
|
|
|
Eukaryotic translation elongation factor 1 alpha 2 |
DEE33, EEF1AL, EF-1-alpha-2, EF1A, EIEE33, HS1, MRD38, STN, STNL |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Congenital epicanthus, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epilepsy, Epileptic encephalopathy, Gastric cancer, Gastroesophageal reflux disease, Hypodontia, Mental retardation, Microcephaly, Hypotonia, Neurodevelopmental disorders, Neurogenic urinary bladder, Non-specifi epileptic encephalopathy, Non-syndromic intellectual disability, Nystagmus, Optic atrophy, Ptosis, Status epilepticus, Stomach neoplasms, Vesicoureteral refluxView all (11 more) |
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2819
|
|
|
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 |
B3Gn-T6, BGnT-6, beta-1,3-Gn-T6, beta3Gn-T6 |
|
|
2820
|
|
|
HIG1 hypoxia inducible domain family member 2A |
HIG2A, RCF1b |
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