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hereditary persistence of fetal hemoglobin - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

hereditary persistence of fetal hemoglobin

MONDO:0020989

Also known as:Disease, Haemoglobin FDisease, Hemoglobin FHEMOGLOBIN F DIS

Overview

The persistence of substantial fetal hemoglobin production into adulthood, usually associated with hemoglobinopathies due to mutations in the alpha and/or beta chain of hemoglobin.

Diagnosis

Biomarker and diagnostic research for hereditary persistence of fetal hemoglobin has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for hereditary persistence of fetal hemoglobin.

142 publications have been identified in PubMed for hereditary persistence of fetal hemoglobin. Research spans Review / Meta-Analysis (34%), Basic Science / Preclinical (20%), and Epidemiology / Natural History (18%).

Research Type	Count	% of Total
Research summaries	48	34%

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 5:51 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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hereditary persistence of fetal hemoglobin

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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