RS80338720 SLC25A13
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Neonatal intrahepatic cholestasis due to citrin deficiency
Citrin deficiency
Citrullinemia type II
Citrullinemia
type II
adult-onset
SLC25A13-related disorder
Adult-onset citrullinemia type I
CITRIN DEFICIENCY
NEONATAL ONSET
Malignant lymphoma
large B-cell
diffuse
Neonatal intrahepatic cholestasis due to citrin deficiency
Citrin deficiency
Other Variants in SLC25A13