RS770171865 PSAP
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Associated Conditions
Sphingolipid activator protein 1 deficiency
Metachromatic leukodystrophy
Combined PSAP deficiency
Krabbe disease due to saposin A deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
Gaucher disease due to saposin C deficiency
Sphingolipid activator protein 1 deficiency
Metachromatic leukodystrophy
Combined PSAP deficiency
Krabbe disease due to saposin A deficiency
Parkinson disease 24
autosomal dominant
susceptibility to
Other Variants in PSAP