Hereditary spherocytosis

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Hereditary spherocytosis

ORPHA:822Disease

Also called Minkowski-Chauffard disease

What it is

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.

Key facts

Prevalence
1-5 / 10 000 (Europe)
Age of onset
All ages
Inheritance
Autosomal dominant, Autosomal recessive
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Genes

ANK1Disease-causing germline mutation(s)
EPB42Disease-causing germline mutation(s)
SLC4A1Disease-causing germline mutation(s)
SPTA1Disease-causing germline mutation(s)
SPTBDisease-causing germline mutation(s)

ICD-10 codes

D58.0ICD-10 names this disease exactly

Cross-references

GARD 6639MEDDRA 10019904MESH D013103MONDO 0019350OMIM 182900OMIM 270970OMIM 612653OMIM 612690OMIM 616649UMLS C0037889

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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