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Hemoglobin C disease

Orpha number ORPHA2132
Synonym(s) -
Prevalence -
Inheritance Autosomal recessive
Age of onset All ages
ICD-10
  • D58.2
ICD-O -
OMIM -
UMLS
  • C0019021
MeSH
  • D006445
MedDRA
  • 10018883

Summary

Hemoglobin C disease (HbC) is a hemoglobinopathy characterized by production of abnormal variant hemoglobin known as hemoglobin C, with no or mild clinical manifestations (hemolytic anemia).


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