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syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome

MONDO:0014069

Also known as:Synactyly-camptodactyly and clinodactyly of fifth fingers-bifid halluces syndromeWahab syndromecamptodactyly, clinodactyly, syndactyly, and bifid toe syndrome

Overview

GeneticsAutosomal dominant

Clinical Presentation

Features include: Camptodactyly, Short foot, Short palm, and Short metacarpal and 5 more.

Organ System	Phenotype Count	Example Features
Arms and legs	1	Short foot

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Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

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 syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome.

46 publications have been identified in PubMed for syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome. Research spans Review / Meta-Analysis (28%), Basic Science / Preclinical (22%), and Clinical Trial Publication (17%).

Research Type	Count	% of Total
Research summaries	13	28%

Data assembled from 5 of 12 sources · Last updated Sep 18, 2026, 1:50 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:615170

Orphanet

European rare disease database

Orphanet:357332

GARD

Genetic and Rare Diseases Info Center

GARD:17551

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
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syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome

Overview

Clinical Presentation

Explore clinical features

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications