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Disease Ontology Browser
hereditary spherocytosis (DOID:12971)
Synonyms: Congenital spherocytic hemolytic anemia; Minkowski Chauffard syndrome; spherocytic anemia
Alt IDs: OMIM:182900, OMIM:270970, OMIM:612653, OMIM:612690, 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 (14)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory