RS1431844269 PSAP
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Associated Conditions
Sphingolipid activator protein 1 deficiency
Combined PSAP deficiency
Metachromatic leukodystrophy
Krabbe disease due to saposin A deficiency
Gaucher disease due to saposin C deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
PSAP-related disorder
Sphingolipid activator protein 1 deficiency
Combined PSAP deficiency
Metachromatic leukodystrophy
Krabbe disease due to saposin A deficiency
Gaucher disease due to saposin C deficiency
Parkinson disease 24
Other Variants in PSAP