- OMIM ID
-
611721
- OMIM term:
- COMBINED SAPOSIN DEFICIENCY
- Alternative terms:
-
PROSAPOSIN DEFICIENCY; PSAPD
COMBINED SAP DEFICIENCY
- (∗) Location:
- 10q22.1
- (†) Associated OMIM genes:
- PSAP SAPOSIN A, INCLUDED; SAPA, INCLUDED
- (‡) Associated MGI genes:
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