Spastic ataxia, dysarthria due to glutaminase deficiency

disorder

SNOMED 1255323007CUI C5681336

Overview

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

Related Conditions

Inherited metabolic disorder of nervous system(parent)

Chronic nervous system disease(parent)

Chronic metabolic disease(parent)

Disturbance of glutamine metabolism(parent)

Global developmental delay(parent)

Developmental hereditary disorder(parent)

Hereditary ataxia(parent)

Quick Facts

SNOMED CT: 1255323007
UMLS CUI: C5681336
Fully Specified Name: Spastic ataxia, dysarthria due to glutaminase 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.