← Back to Conditions

Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation

disorder
SNOMED 1260354005CUI C5787885

Overview

Frontotemporal dementia due to chromosome 9 open reading frame 72 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
1260354005
UMLS CUI
C5787885
Fully Specified Name
Frontotemporal dementia due to C9orf72 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.

Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation — Symptoms, Testing & Specialists | Healos | Ltrl