Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency

disorder

SNOMED 782828005CUI C5190633

Overview

Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Disorder of branched-chain amino acid metabolism(parent)

Global developmental delay(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 782828005
UMLS CUI: C5190633
Fully Specified Name: Developmental delay due to methylmalonate semialdehyde dehydrogenase 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.