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Summary Literature (0)
MIM:612690 - SPHEROCYTOSIS, TYPE 5; SPH5

Xenbase Genes: epb42

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012985 - hereditary spherocytosis type 5
MONDO:0019350 - hereditary spherocytosis

Disease Ontology (DO):
DOID:0110920 - hereditary spherocytosis type 5