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Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

Disease Export to PDF
Name:
Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
Description:
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.
ORPHAcode:
46532
Synonyms:
HPFH-beta-thalassemia syndrome
XREF(s):
Orphanet
OMIM
OMIM
OMIM
OMIM
OMIM
ICD-10
Analyte(s):
HBB
HBG1
HBG2
KLF1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14