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Disease Ontology Browser
hereditary spherocytosis (DOID:12971)
Alliance: disease page
Synonyms: Congenital spherocytic hemolytic anemia; Minkowski Chauffard syndrome; spherocytic anemia
Alt IDs: ICD10CM:D58.0, ICD9CM:282.0, MESH:D013103, NCI:C97074, ORDO:822, UMLS_CUI:C0037889
Definition: A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape.

Disease References using Mouse Models (15)
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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04/16/2024
MGI 6.23 		The Jackson Laboratory