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Summary Literature (0)
MIM:266120 - URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO

Xenbase Genes: nt5c3a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009946 - hemolytic anemia due to pyrimidine 5' nucleotidase deficiency

Disease Ontology (DO):
DOID:583 - hemolytic anemia