- OMIM ID
-
179700
- OMIM term:
- RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS
- Alternative terms:
-
HIGH RED CELL PHOSPHATIDYLCHOLINE HEMOLYTIC ANEMIA; HPCHA
PHOSPHATIDYLCHOLINE RED CELL MEMBRANE DISORDER
LEAKY RED CELL SYNDROME
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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