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digitotalar dysmorphism (DA1) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

digitotalar dysmorphism

MONDO:0015240

Also known as:DA1arthrogryposis multiplex congenita distal type 1distal arthrogryposis type 1

Overview

Digitotalar dysmorphism, also known as distal arthrogryposis type 1 (DA1), is an autosomal dominant congenital anomaly characterized by contractures of the distal regions of the hands and feet with no facial involvement or any additional anomalies. It is the most common type of distal arthrogryposis.

ResearchLimited published research (1 article)

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

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 digitotalar dysmorphism.

1 publication has been identified in PubMed for digitotalar dysmorphism. Research spans Basic Science / Preclinical (100%).

Recent Publications

Iyer A (2024). [PMID: 38438057](https://pubmed.ncbi.nlm.nih.gov/38438057/). *Gene*. [Basic Science / Preclinical]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:48 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:1146

GARD

Genetic and Rare Diseases Info Center

GARD:787

Questions for Your Care Team

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digitotalar dysmorphism

Overview

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team