Pages that link to "Biology:SLC5A1"
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The following pages link to Biology:SLC5A1:
Displayed 22 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Medicine:Fanconi–Bickel syndrome (← links)
- Medicine:Congenital disorder of glycosylation type IIc (← links)
- Medicine:Lysinuric protein intolerance (← links)
- Medicine:Iminoglycinuria (← links)
- Medicine:Pendred syndrome (← links)
- Medicine:Acrodermatitis enteropathica (← links)
- Medicine:Atelosteogenesis, type II (← links)
- Medicine:Gitelman syndrome (← links)
- Medicine:Autosomal recessive multiple epiphyseal dysplasia (← links)
- Medicine:Diastrophic dysplasia (← links)
- Medicine:Glucose-galactose malabsorption (← links)
- Medicine:Arterial tortuosity syndrome (← links)
- Medicine:Cystinuria (← links)
- Medicine:Hartnup disease (← links)
- Medicine:Salla disease (← links)
- Medicine:Hyperinsulinemic hypoglycemia (← links)
- Medicine:Genetic disorder (← links)
- Medicine:Nonsyndromic deafness (← links)
- Medicine:List of OMIM disorder codes (← links)
- Medicine:Multiple epiphyseal dysplasia (← links)
- Medicine:Achondrogenesis type 1B (← links)
- Medicine:Allan–Herndon–Dudley syndrome (← links)
