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hereditary spherocytosis

Disease Summary
Associated Targets (8)
Tbio

5

Tclin

2

Tchem

1


GARD Rare
Mondo Description Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.
Disease Ontology Description A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape.
Mondo Term and Equivalent IDs
MONDO:0019350:  hereditary spherocytosis
COHD:24909: 
GARD:0006639: 
ICD10:D58.0: 
ICD9:282.0: 
MESH:D013103: 
NCIT:C97074: 
Orphanet:822: 
SCTID:55995005: 
UMLS:C0037889: 
UMLS:CN206031: