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familial multiple fibrofolliculoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial multiple fibrofolliculoma

MONDO:0018070

Also known as:multiple fibrofolliculoma familial

Overview

Familial multiple fibrofolliculoma is a genodermatosis characterized by the presence of multiple hamartomas of the hair follicle. It has been described in one family so far.

Diagnosis

Biomarker and diagnostic research for familial multiple fibrofolliculoma 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 familial multiple fibrofolliculoma.

10 publications have been identified in PubMed for familial multiple fibrofolliculoma. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (20%), and Diagnostic / Biomarker (10%).

Research Type	Count	% of Total
Patient case studies	5	50%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 3:08 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:338

GARD

Genetic and Rare Diseases Info Center

GARD:3831

Questions for Your Care Team

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familial multiple fibrofolliculoma

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications