Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

Orpha code: 46532OMIM code: 613566

Definition

Hereditary persistence of fetal hemoglobin (HPFH) associated with beta-thalassemia (see this term) is characterized by high hemoglobin (Hb) F levels and an increased number of fetal-Hb-containing-cells.

Disease data
Classification

Disease

Synonyms
HPFH-beta-thalassemia syndrome
HPFH - beta-talasemia
ORPHA code
46532
OMIM code
613566
ICD10 code
D56.4
ICD11 code
3A50.4

No additional description.

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