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.

Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency — Symptoms, Testing & Specialists | Healos | Healos