Adenosylcobalamin and methylcobalamin synthesis defect

disorder

SNOMED 4409006CUI C0268591

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Cobalamin D disease(child)

Cobalamin A disease(child)

Cobalamin C disease(child)

Inherited methylmalonic acidemia AND homocystinuria(child)

Methylmalonic acidemia(parent)

Quick Facts

SNOMED CT: 4409006
UMLS CUI: C0268591
Fully Specified Name: Adenosylcobalamin and methylcobalamin synthesis defect (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.