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tracheobronchopathia osteochondroplastica - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

tracheobronchopathia osteochondroplastica

MONDO:0008587

Also known as:tracheopathia osteoplasticacartilaginous or bony projections into the tracheobronchial lumentracheobronchopathia osteoplastica

Overview

Tracheobronchopathia osteochondroplastica (TO) is an idiopathic and benign disease of the large airways characterized by submucosal osteocartilaginous nodules presenting in the trachea with or without the involvement of the major bronchi.

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 very common findings: Tracheal calcification and Productive cough; and common findings: Fever, Pneumonia, Recurrent respiratory infections, and Tracheal stenosis and others. 23 total HPO annotations.

Organ System	Phenotype Count	Example Features
Lungs and breathing	9	Pneumonia, Recurrent respiratory infections, Upper airway obstruction

Prognosis

Phenotype severity distribution: 2 very common features, 11 common features.

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 tracheobronchopathia osteochondroplastica.

21 publications have been identified in PubMed for tracheobronchopathia osteochondroplastica. Research spans Case Report / Case Series (81%), Other (10%), and Review / Meta-Analysis (5%).

Research Type	Count	% of Total
Patient case studies	17	81%

Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 3:30 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:189961

Orphanet

European rare disease database

Orphanet:3348

GARD

Genetic and Rare Diseases Info Center

GARD:5235

Questions for Your Care Team

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tracheobronchopathia osteochondroplastica

Overview

Clinical Presentation

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Questions for Your Care Team

Questions for Your Care Team

Explore clinical features

Recent Publications

tracheobronchopathia osteochondroplastica

Overview

Clinical Presentation

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Explore clinical features

Recent Publications