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taurodontia-absent teeth-sparse hair syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

taurodontia-absent teeth-sparse hair syndrome

MONDO:0010102

Also known as:taurodontia, absent teeth, and sparse hairtaurodontia, absent teeth, sparse hair syndrometeeth, congenital absence of, with taurodontia and sparse hair

Overview

This syndrome is characterized by congenital absence of the teeth, and sparse or absent hair. Taurodontia is also present in the majority of cases. The syndrome has been described in less than 15 patients from different families.

Diagnosis

Biomarker and diagnostic research for taurodontia-absent teeth-sparse hair syndrome 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 taurodontia-absent teeth-sparse hair syndrome.

200 publications have been identified in PubMed for taurodontia-absent teeth-sparse hair syndrome. Kisho has analyzed 66 by research type. Research spans Review / Meta-Analysis (33%), Other (26%), and Basic Science / Preclinical (15%).

Research Type	Count	% of Total
Research summaries	22	33%

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 3:17 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:272980

Orphanet

European rare disease database

Orphanet:2731

GARD

Genetic and Rare Diseases Info Center

GARD:5118

Questions for Your Care Team

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taurodontia-absent teeth-sparse hair syndrome

Overview

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications