187288
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Signaling receptor and transporter of retinol STRA6 |
MCOPCB8, MCOPS9, PP14296, SLC69A1 |
Curated: Anophthalmia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Cardiovascular abnormalities, Central nervous system cancer, Colobomatous microphthalmia, Congenital heart disease, Craniofacial abnormalities, Glioblastoma, Glioma, Congenital heart defects, Intellectual developmental disorder, Lung disease, Microphthalmia, Microphthalmia, syndromic 9, Microphthalmia, isolated, with coloboma 8
Unreviewed: Alveolar capillary dysplasia, Anemia, Annular pancreas, Aortic Coarctation, Atrial Septal Defect, Blepharophimosis, Carcinogenesis, Cardiac Defects, Cardiovascular Abnormalities, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Complete Atrioventricular Canal Defect, Congenital Atresia Of Pulmonary Artery, Congenital Camptodactyly, Congenital diaphragmatic hernia, Congenital heart defect, Congenital ocular coloboma, Conotruncal cardiac defect, Cryptorchidism, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diaphragmatic Eventration, Diaphragmatic malformations, Disorder Of Eye, Dwarfism, Gestational diabetes, Heart disease, Heart Diseases, Hepatocellular carcinoma, Hereditary breast and ovarian cancer syndrome, Horseshoe Kidney, Hydronephrosis, Lung Diseases, Malignant Neoplasm, Malrotation Of Kidney, Matthew-Wood Syndrome, Mental retardation, Metabolic Syndrome, Micrognathism, Microphthalmia With Coloboma, Microphthalmos, Myocardial Infarction, Neoplasms, Osteoporosis, Pancreatitis, Papillary thyroid cancer, Patent ductus arteriosus, Pelvic kidney, Pulmonary hypoplasia, Pulmonary Stenosis, Renal hypoplasia, Rheumatoid arthritis, Single Ventricle Defect, Stomach Carcinoma, Stomach Neoplasms, Syndromic microphthalmia, Tetralogy of Fallot, Trichohepatoenteric Syndrome, Uterine Anomalies, Ventricular septal defect, Vesicoureteral Reflux
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