|
671
|
|
|
Sodium channel epithelial 1 subunit gamma |
BESC3, ENaCg, ENaCgamma, LDLS2, PHA1, PHA1B3, SCNEG |
Bronchiectasis, Ciliopathies, Colorectal cancer, Cystic fibrosis, Cystic fibrosis of pancreas, Bronchitis, Hyperaldosteronism, Hyperpotassemia and hypertension, Hypertension, Kidney disease, Liddle syndrome, Lung diseases, Metabolic alkalosis, Myocardial infarction, Pseudohypoaldosteronism, Pulmonary cystic fibrosis, Renal insufficiencyView all (2 more) |
|
672
|
|
|
Synthesis of cytochrome C oxidase 1 |
MC4DN4, SCOD1 |
Anemia, Cardioencephalomyopathy, Cytochrome-c oxidase deficiency, Developmental delay, Epileptic encephalopathy, Fanconi syndrome, Fatal cytochrome c oxidase deficiency, Hearing loss, Heart diseases, High palate, Hypertrophic cardiomyopathy, Leukoencephalopathy, Liver failure, Mental retardation, Mitochondrial diseases, Mitochondrial electron transport chain deficiencies, Mitochondrial respiratory chain deficiencies, Motor delay, Optic atrophy, Oxidative phosphorylation deficiency, Phosphate diabetes, Ptosis, Renal tubular disorder, Retinitis pigmentosaView all (9 more) |
|
673
|
|
|
Sterol carrier protein 2 |
NLTP, NSL-TP, SCOX, SCP-2, SCP-CHI, SCP-X, SCPX |
|
|
674
|
|
|
Secretin |
- |
|
|
675
|
|
|
Secretin receptor |
SECR, SR |
|
|
676
|
|
|
Syndecan 1 |
CD138, SDC, SYND1, syndecan |
|
|
677
|
|
|
Serine racemase |
ILV1, ISO1 |
|
|
678
|
|
|
Syndecan 4 |
SYND4 |
|
|
679
|
|
|
Syndecan binding protein |
MDA-9, MDA9, SDCBP1, ST1, SYCL, TACIP18 |
|
|
680
|
|
|
Succinate dehydrogenase complex flavoprotein subunit A |
CMD1GG, FP, MC2DN1, NDAXOA, PGL5, PPGL5, SDH1, SDH2, SDHF |
Adrenal gland pheochromocytoma, Anemia, Aniridia, Arthritis, Astrocytoma, Attention deficit hyperactivity disorder, Hereditary cancer syndrome, Capillary hemangioma of retina, Carcinoma, Cardiomyopathy, Carney triad, Central nervous system demyelination, Cerebellar ataxia, Colonic neoplasms, Congestive heart failure, Cranial nerve compression, Dementia, Developmental delay, Developmental regression, Dilated cardiomyopathy, Disorder of skeletal muscle, Distal amyotrophy, Dwarfism, Dysarthria, Dysphagia, Encephalopathy, Episodic paroxysmal anxiety, Esophagus neoplasm, External ophthalmoplegia, Extra-adrenal pheochromocytoma, Gastrointestinal stromal tumor, Glomerulonephritis, Glomerulosclerosis, Hearing loss, Hereditary paraganglioma-pheochromocytoma syndromes, Hereditary pheochromocytoma-paraganglioma, Hypercalcemia, Hypertensive retinopathy, Hypertrichosis, Hypertrophic cardiomyopathy, Impaired cognition, Mental retardation, Intestinal neoplasms, Intestinal obstruction, Isolated succinate-coq reductase deficiency, Left ventricular hypertrophy, Left ventricular noncompaction, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Lipoatrophy, Lipodystrophy, Mitochondrial complex deficiency, Mood swings, Motor delay, Myoclonic seizures, Myopathy, Necrotizing encephalomyelopathy, Hypotonia, Nervous system diseases, Noncompaction cardiomyopathy, Nystagmus, Optic atrophy, Osteoarthrosis deformans, Palmoplantar keratoderma, Panic disorder, Paraganglioma, Paraganglioma of head and neck, Ptosis, Pulmonary chondroma, Pulsatile tinnitus, Rectal neoplasms, Renal carcinoma, Respiratory failure, Retinitis pigmentosa, Sarcoma, Schizophrenia, Sinus tachycardia, Spastic tetraparesis, Stomach neoplasms, Strabismus, Ventricular septal defect, Vesicoureteral reflux, Vocal cord paralysisView all (69 more) |
