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inborn disorder of lysine, hydroxylysine, and tryptophan metabolism - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

inborn disorder of lysine, hydroxylysine, and tryptophan metabolism

MONDO:0800157

Overview

A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of lysine, hydroxylysine, and/or tryptophan.

ResearchLimited published research (3 articles)

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 lysine, hydroxylysine, and tryptophan metabolism.

3 publications have been identified in PubMed for inborn disorder of lysine, hydroxylysine, and tryptophan metabolism. Research spans Review / Meta-Analysis (67%) and Case Report / Case Series (33%).

Recent Publications

Gragnaniello V (2025). [PMID: 40361251](https://pubmed.ncbi.nlm.nih.gov/40361251/). *Ital J Pediatr*. [Case Report / Case Series]
Tarr JD (2025). [PMID: 39953653](https://pubmed.ncbi.nlm.nih.gov/39953653/). *J Inherit Metab Dis*. [Review / Meta-Analysis]
Gemici Karaaslan B (2025). [PMID: 39957310](https://pubmed.ncbi.nlm.nih.gov/39957310/). *J Inherit Metab Dis*. [Review / Meta-Analysis]

Data assembled from 2 of 12 sources · Last updated Sep 21, 2026, 4:54 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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inborn disorder of lysine, hydroxylysine, and tryptophan metabolism

Overview

Research Landscape

Recent Publications

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team