HPDL-related Leigh-like encephalopathy

disorder

SNOMED 1303585005CUI C5816791

Overview

HPDL-related Leigh-like encephalopathy is a disorder.

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

Related Conditions

Hereditary degenerative disease of central nervous system(parent)

Chronic nervous system disease(parent)

Developmental hereditary disorder(parent)

Spastic syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 1303585005
UMLS CUI: C5816791
Fully Specified Name: Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome (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.