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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,
Echinobase Genes :
MIM:611804 - elliptocytosis 1; el1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hematopoietic system disease (is_a)