Disease & disorder

hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

MONDO:0018749

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

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome. Results are keyword matches, not yet verified disease-to-outbreak relationships.

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms1
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Background context

hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome

Wikidata Q56014196 ↗
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.