- OMIM ID
-
266120
- OMIM term:
- URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO
- Alternative terms:
-
HEMOLYTIC ANEMIA DUE TO UMPH1 DEFICIENCY
PYRIMIDINE 5-PRIME NUCLEOTIDASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO
HEMOLYTIC ANEMIA DUE TO P5N DEFICIENCY
P5N DEFICIENCY
UMPH1 DEFICIENCY
- (∗) Location:
- 7p14.3
- (†) Associated OMIM genes:
- NT5C3
- (‡) Associated MGI genes:
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