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Summary Literature (0)
MIM:206400 - ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRIN METABOLISM

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008790 - anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism

Disease Ontology (DO):
DOID:2861 - congenital nonspherocytic hemolytic anemia