Genetic disorder, membrane: Solute carrier disorders | |
|---|---|
| 1-10 | SLC1A3 (Episodic ataxia 6) • SLC2A1 (De Vivo disease) • SLC2A5 (Fructose malabsorption) • SLC2A10 (Arterial tortuosity syndrome) • SLC3A1 (Cystinuria) • SLC4A1 (Hereditary spherocytosis 4/Hereditary elliptocytosis 4) • SLC4A11 (Congenital endothelial dystrophy type 2, Fuchs' dystrophy 4) • SLC5A1 (Glucose-galactose malabsorption) • SLC5A2 (Renal glycosuria) • SLC5A5 (Thyroid dyshormonogenesis type 1) • SLC6A19 (Hartnup disease) • SLC7A7 (Lysinuric protein intolerance) • SLC7A9 (Cystinuria) |
| 11-20 | SLC11A1 (Crohn's disease) • SLC12A3 (Gitelman syndrome) • SLC16A1 (HHF7) • SLC16A2 (Allan–Herndon–Dudley syndrome) • SLC17A5 (Salla disease) • SLC17A8 (DFNA25) |
| 21-40 | |