Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

nonsyndromic congenital nail disorder 6 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

nonsyndromic congenital nail disorder 6

MONDO:0007135

Also known as:nonsyndromic congenital nail disorder type 6NDNC6absent nails and dystrophic nails

Overview

GeneticsAutosomal dominant

ResearchLimited published research (5 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 sometimes findings: Tapered distal phalanges of finger. 5 total HPO annotations.

Organ System	Phenotype Count	Example Features
Skin	2	Nail dysplasia, Nail dystrophy
Pregnancy and birth

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 nonsyndromic congenital nail disorder 6.

5 publications have been identified in PubMed for nonsyndromic congenital nail disorder 6. Research spans Case Report / Case Series (60%), Other (20%), and Review / Meta-Analysis (20%).

Recent Publications

Tanti S (2026). [PMID: 41737087](https://pubmed.ncbi.nlm.nih.gov/41737087/). *Cureus*. [Case Report / Case Series]
Zhang Q (2025). [PMID: 40620857](https://pubmed.ncbi.nlm.nih.gov/40620857/). *Front Pediatr*. [Case Report / Case Series]
Shaheen EA (2025). [PMID: 39845463](https://pubmed.ncbi.nlm.nih.gov/39845463/). *JAAD Case Rep*. [Case Report / Case Series]
Maarouf S (2025). [PMID: 39659087](https://pubmed.ncbi.nlm.nih.gov/39659087/). *Pediatr Dermatol*. [Review / Meta-Analysis]
Mondal R (2024). [PMID: 39469427](https://pubmed.ncbi.nlm.nih.gov/39469427/). *Med Res Arch*. [Other]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 4:33 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:107000

GARD

Genetic and Rare Diseases Info Center

GARD:15040

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

nonsyndromic congenital nail disorder 6

Overview

Clinical Presentation

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Explore clinical features