Frontotemporal dementia due to valosin containing protein mutation

disorder

SNOMED 1260353004CUI C5787884

Overview

Frontotemporal dementia due to valosin containing protein mutation is a disorder.

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

Related Conditions

Cerebral degeneration associated with another disorder(parent)

Frontotemporal dementia(parent)

Dementia due to chromosomal anomaly(parent)

Quick Facts

SNOMED CT: 1260353004
UMLS CUI: C5787884
Fully Specified Name: Frontotemporal dementia due to VCP mutation (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.