Pages that link to "SLC17A8"
From WikiMD's Wellness Encyclopedia
← SLC17A8
The following pages link to SLC17A8:
Displaying 18 items.
- Gitelman syndrome (← links | edit)
- Hereditary elliptocytosis (← links | edit)
- Pendred syndrome (← links | edit)
- Cystinuria (← links | edit)
- Acrodermatitis enteropathica (← links | edit)
- Lysinuric protein intolerance (← links | edit)
- Allan–Herndon–Dudley syndrome (← links | edit)
- Fanconi–Bickel syndrome (← links | edit)
- Atelosteogenesis type 2 (← links | edit)
- SLC35C1-CDG (CDG-IIc) (← links | edit)
- Glucose transporter type 1 deficiency syndrome (← links | edit)
- Adenine nucleotide translocator (← links | edit)
- SCN4B (← links | edit)
- MCOLN1 (← links | edit)
- SLC13A3 (← links | edit)
- GLUT5 (← links | edit)
- Sodium/myo-inositol cotransporter (← links | edit)
- SLC17A8 (transclusion) (← links | edit)