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disorder of methionine catabolism - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

disorder of methionine catabolism

MONDO:0000351

Also known as:hypermethioninemiainborn error of methionine catabolic processinborn methionine catabolic process disorder

Overview

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

Diagnosis

Biomarker and diagnostic research for disorder of methionine catabolism 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 disorder of methionine catabolism.

107 publications have been identified in PubMed for disorder of methionine catabolism. Research spans Basic Science / Preclinical (60%), Review / Meta-Analysis (18%), and Case Report / Case Series (7%).

Research Type	Count	% of Total
Laboratory research	64	60%

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 2:19 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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disorder of methionine catabolism

Overview

Diagnosis

Research Landscape

Medical References

Subtypes

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Questions for Your Care Team

Questions for Your Care Team

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