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inborn disorder of methionine cycle and sulfur amino acid metabolism - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

inborn disorder of methionine cycle and sulfur amino acid metabolism

MONDO:0019222

Also known as:cytosolic methyl group transfer or sulfur amino acid metabolism disordercytosolic methyl group transfer or sulphur amino acid metabolism disorderinborn error of sulfur amino acid metabolic process

Overview

An inherited metabolic disease that is has its basis in the disruption of sulfur amino acid metabolic process.

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 methionine cycle and sulfur amino acid metabolism.

171 publications have been identified in PubMed for inborn disorder of methionine cycle and sulfur amino acid metabolism. Research spans Basic Science / Preclinical (50%), Review / Meta-Analysis (25%), and Epidemiology / Natural History (14%).

Research Type	Count	% of Total
Laboratory research	85	50%

Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 12:40 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:79173

GARD

Genetic and Rare Diseases Info Center

GARD:18953

Questions for Your Care Team

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inborn disorder of methionine cycle and sulfur amino acid metabolism

Overview

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications