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Disease Ontology Browser
hereditary elliptocytosis (DOID:2373)
Alliance: disease page
Synonyms: Congenital elliptocytosis; ovalocytosis
Alt IDs: OMIM:130600, OMIM:611804, ICD10CM:D58.1, ICD9CM:282.1, MESH:D004612, NCI:C35882, ORDO:288, UMLS_CUI:C0013902
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory