PSAP

Prosaposin (sphingolipid activator protein-1)
5660

 

Combined SAP deficiency – 611721

Krabbe disease, atypical – 611722

Metachromatic leukodystrophy due to SAP-b deficiency – 249900

Gaucher disease, atypical – 610539

{Parkinson disease 24, autosomal dominant, susceptibility to} – 619491

 

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