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

Rare Disease

inborn disorder of aspartate family metabolism

MONDO:0037938

Also known as:inborn aspartate family amino acid metabolic process disorderinborn error of aspartate family amino acid metabolic processrare inborn error of aspartate family amino acid metabolic process

Overview

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

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 aspartate family metabolism.

3 publications have been identified in PubMed for inborn disorder of aspartate family metabolism. Research spans Case Report / Case Series (100%).

Recent Publications

Urquiza N (2026). [PMID: 41475179](https://pubmed.ncbi.nlm.nih.gov/41475179/). *Molecular genetics and metabolism*. [Case Report / Case Series]
Lizama-Muñoz A (2026). [PMID: 42099593](https://pubmed.ncbi.nlm.nih.gov/42099593/). *Front Immunol*. [Case Report / Case Series]
Alabbasi L (2024). [PMID: 39156350](https://pubmed.ncbi.nlm.nih.gov/39156350/). *Cureus*. [Case Report / Case Series]

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 9:36 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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inborn disorder of aspartate family metabolism

Overview

Research Landscape

Recent Publications

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team