|
771
|
|
|
Solute carrier family 4 member 1 (Diego blood group) |
AE1, BND3, CD233, CHC, DI, EMPB3, EPB3, FR, RTA1A, SAO, SPH4, SW, WD, WD1, WR |
Anemia, Anorexia, Cholelithiasis, Dehydrated hereditary stomatocytosis, Distal renal tubular acidosis, Distal renal tubular acidosis with anemia, Dwarfism, Elliptocytosis, Fibrinogen deficiency, Gout, Hematological disease, Hereditary cryohydrocytosis with normal stomatin, Hereditary spherocytosis, Hyperbilirubinemia, Hypofibrinogenemia, Isothenuria, Microangiopathic hemolytic anemia, Nephritis, Nephrocalcinosis, Ovalocytosis, Periodic hypokalemic paresis, Periodic paralysis, Pseudohyperkalemia cardiff, Renal tubular acidosis, Renal tubular acidosis, distal, with hemolytic anemia, Renal tubular acidosis, with normal red cell morphology, Restrictive cardiomyopathy, Rickets, Southeast asian ovalocytosis, Spherocytosis, Thrombophilia, XerocytosisView all (17 more) |
|
772
|
|
|
Solute carrier family 4 member 2 |
AE2, BND3L, EPB3L1, HKB3, NBND3, OPTB9 |
|
|
773
|
|
|
Solute carrier family 5 member 1 |
D22S675, NAGT, SGLT-1, SGLT1 |
|
|
774
|
|
|
Solute carrier family 5 member 2 |
SGLT2 |
|
|
775
|
|
|
Smoothelin |
- |
|
|
776
|
|
|
Solute carrier family 5 member 3 |
BCW2, SMIT, SMIT1, SMIT2 |
|
|
777
|
|
|
Solute carrier family 5 member 4 |
DJ90G24.4, SAAT1, SGLT3 |
|
|
778
|
|
|
Solute carrier family 5 member 5 |
NIS, TDH1 |
Benign neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Cholangiocarcinoma, Congenital exomphalos, Developmental delay, Dwarfism, Glioma, Hypersomnia, Hypothyroidism, Intrahepatic cholangiocarcinoma, Kidney neoplasm, Kidney cancer, Liver carcinoma, Macroglossia, Malignant neoplasm, Marfan syndrome, Melanoma, Mental retardation, Neoplasms, Ovarian neoplasm, Ovarian cancer, Prostatic neoplasms, Prostate cancer, Thyroid neoplasm, Thyroid carcinoma, Thyroid dyshormonogenesis, Thyroid gland follicular adenomaView all (14 more) |
|
779
|
|
|
Solute carrier family 6 member 1 |
GABATHG, GABATR, GAT1, MAE, hGAT-1 |
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Angelman syndrome, Autism, Clonic seizures, Developmental delay, Developmental regression, Dysarthria, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Febrile seizures, Hypotonic seizures, Jacksonian seizure, Mental depression, Mental retardation, Myoclonic astatic epilepsy, Myoclonic atonic seizures, Myoclonic-astatic epilepsy, Myoclonic-atonic epilepsy, Neurodevelopmental disorders, Photosensitive tonic-clonic seizures, Schizophrenia, Seizure, Status epilepticusView all (10 more) |
|
780
|
|
|
Solute carrier family 6 member 2 |
NAT1, NET, NET1, SLC6A5 |
Bipolar disorder, Clonic seizures, Hypertension, Hypotonic seizures, Jacksonian seizure, Mental depression, Mitral valve prolapse, Mood disorder, Neurocirculatory asthenia, Postural orthostatic tachycardia syndrome, Schizophrenia, Seizure |
