About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory