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Summary Literature (0)
DOID:2373 - hereditary elliptocytosis

Disease Ontology Definition:A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present.

Synonyms: Congenital elliptocytosis, ovalocytosis

Xenbase Genes : epb41, sptb, gypc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0017319 - hereditary elliptocytosis

MIM:
MIM:130600 - ELLIPTOCYTOSIS 2; EL2
MIM:611804 - ELLIPTOCYTOSIS 1; EL1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hematopoietic system disease (is_a)