SLC5A1

solute carrier family 5 member 1
OMIM: 182380
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glucose/galactose malabsorption (Disorders of glucose transport), Glucose/galactose malabsorption 606824 (Disorders of glucose transport)
R-numbers: R331
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glucose/galactose malabsorption, OMIM:606824