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.

Synonyms: Minkowski-Chauffard disease

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Term information

database cross reference
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ICD-10:D58.0

MeSH:C536356

OMIM:612653

MedDRA:10019904

OMIM:616649

UMLS:C0221409

OMIM:182900

UMLS:C0037889

OMIM:270970

MeSH:D013103

OMIM:612690

notation

ORPHA:822