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

Rare Disease

inborn disorder of tryptophan metabolism

MONDO:0017350

Also known as:inborn error of tryptophan metabolic processinborn tryptophan metabolic process disorderrare inborn error of tryptophan metabolic process

Overview

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

OnsetNEONATAL

Diagnosis

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

10 publications have been identified in PubMed for inborn disorder of tryptophan metabolism. Research spans Diagnostic / Biomarker (30%), Review / Meta-Analysis (20%), and Basic Science / Preclinical (20%).

Research Type	Count	% of Total
Testing and diagnosis research	3	30%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:38 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:289829

GARD

Genetic and Rare Diseases Info Center

GARD:21154

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
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inborn disorder of tryptophan 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