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Summary Literature (0)
MIM:266200 - ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 2; CNSHA2

Xenbase Genes: pklr

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009950 - olfactory bulb plexiform layer

Disease Ontology (DO):
DOID:0111077 - congenital nonspherocytic hemolytic anemia 2