Disease #02041

Official abbreviation -
Name anemia, hemolytic , due to uridine 5-prime monophosphate hydrolase deficiency
OMIM ID 266120
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NT5C3
Associated tissues -
Disease features -
Remarks -