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Hereditary spherocytosis

Disease Export to PDF
Name:
Hereditary spherocytosis
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.
ORPHAcode:
822
Synonyms:
Minkowski-Chauffard disease
XREF(s):
Orphanet
MeSH
MeSH
MedDRA
ICD-10
OMIM
OMIM
OMIM
OMIM
OMIM
Analyte(s):
SLC4A1
SPTA1
SPTB
ANK1
EPB42
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14