A sphingolipidosis caused by variants in the PSAP gene. Clinical and biochemical features vary based on the location of variants within the gene and their molecular impact. [ https://clinicalgenome.org/affiliation/50009/ ]

This is just here as a test because I lose it

Term information

Subsets

rare, inferred_rare

creator

https://orcid.org/0000-0001-5208-3432

id

MONDO:0100517

Term relations

Subclass of: