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inborn disorder of ornithine metabolism - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

inborn disorder of ornithine metabolism

MONDO:0017356

Also known as:disorder of ornithine metabolisminborn error of ornithine metabolic processinborn ornithine metabolic process disorder

Overview

An inherited metabolic disease that is has its basis in the disruption of ornithine metabolic process.

Diagnosis

Biomarker and diagnostic research for inborn disorder of ornithine metabolism 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 inborn disorder of ornithine metabolism.

129 publications have been identified in PubMed for inborn disorder of ornithine metabolism. Kisho has analyzed 48 by research type. Research spans Case Report / Case Series (23%), Review / Meta-Analysis (21%), and Epidemiology / Natural History (21%).

Research Type	Count	% of Total
Patient case studies	11	23%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:41 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:289869

GARD

Genetic and Rare Diseases Info Center

GARD:21158

Questions for Your Care Team

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inborn disorder of ornithine metabolism

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications