DOID:12971 - hereditary spherocytosis
Disease Ontology Definition:A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape.
Synonyms: Congenital spherocytic hemolytic anemia, Minkowski Chauffard syndrome, spherocytic anemia
|MONDO:0019350 - hereditary spherocytosis|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : sptb, slc4a1, ank1, epb42
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): congenital hemolytic anemia (is_a)