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

anodontia - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

anodontia

MONDO:0008797

Also known as:complete absence of teethdevelopmental absence of toothtotal anodontia of permanent and deciduous teeth

Find Clinical TrialsTrials

Overview

Anodontia is an extreme developmental dental anomaly characterized by the complete absence of all teeth.

GeneticsAutosomal recessive

Clinical Trials1 registered

Clinical Presentation

Features include: Anodontia.

Explore clinical features

Diagnosis

Biomarker and diagnostic research for anodontia 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.

1 clinical trial registered. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.

203 publications have been identified in PubMed for anodontia. Kisho has analyzed 54 by research type. Research spans Epidemiology / Natural History (33%), Review / Meta-Analysis (24%), and Case Report / Case Series (22%).

Research Type	Count	% of Total
Disease patterns and progression	18

Data assembled from 6 of 12 sources · Last updated Sep 18, 2026, 7:12 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:206780

Orphanet

European rare disease database

Orphanet:99797

GARD

Genetic and Rare Diseases Info Center

GARD:5818

Questions for Your Care Team

→Should my partner and I meet with a genetic counselor to discuss carrier status and family planning?
→Are any of the 1 active clinical trial a good fit for my situation?
→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

anodontia

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications