Pelizaeus-Merzbacher disease, connatal variant

disorder

SNOMED 59636002CUI C0393656

Overview

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

Related Conditions

Pelizaeus-Merzbacher disease(parent)

Congenital degeneration of nervous system(parent)

Congenital anomaly of central nervous system(parent)

X-linked recessive hereditary disease(parent)

Quick Facts

SNOMED CT: 59636002
UMLS CUI: C0393656
Fully Specified Name: Pelizaeus-Merzbacher disease, connatal variant (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.