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

Rare Disease

inborn disorder of serine family metabolism

MONDO:0019239

Also known as:inborn disorder of serine or glycine metabolisminborn error of serine family amino acid metabolic processinborn serine family amino acid metabolic process disorder

Overview

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

Diagnosis

Biomarker and diagnostic research for inborn disorder of serine family 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 serine family metabolism.

131 publications have been identified in PubMed for inborn disorder of serine family metabolism. Research spans Basic Science / Preclinical (73%), Gene Therapy / Novel Therapeutics (7%), and Epidemiology / Natural History (6%).

Research Type	Count	% of Total
Laboratory research	95	73%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 12:49 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:79194

GARD

Genetic and Rare Diseases Info Center

GARD:18968

Questions for Your Care Team

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inborn disorder of serine family metabolism

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications