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brachydactyly type A3 (BDA3) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

brachydactyly type A3

MONDO:0007217

Also known as:BDA3brachydactyly-clinodactylybrachymesophalangy V

Overview

GeneticsAutosomal dominant

ResearchLimited published research (6 articles)

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include: Type A brachydactyly, Short middle phalanx of the 5th finger, Clinodactyly of the 5th finger, and Cone-shaped epiphysis and 1 more.

Organ System	Phenotype Count	Example Features
Arms and legs	3	Short middle phalanx of the 5th finger, Clinodactyly of the 5th finger, Rhomboid or triangular shaped 5th finger middle phalanx

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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 brachydactyly type A3.

6 publications have been identified in PubMed for brachydactyly type A3. Research spans Case Report / Case Series (33%), Basic Science / Preclinical (33%), and Epidemiology / Natural History (33%).

Recent Publications

Nerakh G (2025). [PMID: 40657982](https://pubmed.ncbi.nlm.nih.gov/40657982/). *Clin Dysmorphol*. [Case Report / Case Series]
Wang X (2025). [PMID: 40589517](https://pubmed.ncbi.nlm.nih.gov/40589517/). *Front Endocrinol (Lausanne)*. [Basic Science / Preclinical]
Wu HH (2025). [PMID: 41231904](https://pubmed.ncbi.nlm.nih.gov/41231904/). *PLoS One*. [Epidemiology / Natural History]
Zhang W (2025). [PMID: 41238365](https://pubmed.ncbi.nlm.nih.gov/41238365/). *BMJ Open*. [Epidemiology / Natural History]
Kang MJ (2025). [PMID: 41601935](https://pubmed.ncbi.nlm.nih.gov/41601935/). *Front Endocrinol (Lausanne)*. [Basic Science / Preclinical]

Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 11:53 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:112700

Orphanet

European rare disease database

Orphanet:93393

GARD

Genetic and Rare Diseases Info Center

GARD:963

Questions for Your Care Team

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brachydactyly type A3

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team