Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency

disorder

SNOMED 765137006CUI C4707328

Overview

Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Methylmalonic acidemia(parent)

Inborn error of metabolism(parent)

Quick Facts

SNOMED CT: 765137006
UMLS CUI: C4707328
Fully Specified Name: Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.