Frontotemporal dementia with gene located on 3p11

disorder

SNOMED 702393003CUI C1833296

Overview

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Aggression

HP:0000718

Cerebral cortex atrophy

HP:0002120

Difficulty making arithmetical calculations

HP:0002442

Dystonic movements

HP:0001332

Extensor plantar responses

HP:0003487

Frontal release signs

HP:0000743

Frontotemporal dementia

HP:0002145

Gait disturbance

HP:0001288

Impulse control disorders

HP:0000734

Inappropriate behavior

HP:0000719

Increase in astrocyte number

HP:0002446

Increased reflexes

HP:0001347

Jerking

HP:0001336

Lack of feeling, emotion, interest

HP:0000741

Lack of insight

HP:0000757

Loss of speech

HP:0002371

Memory loss

HP:0002354

Mouthing

HP:0000710

Muscle rigidity

HP:0002063

Mutism

HP:0002300

Neuronal loss in CNS

HP:0002529

Orofacial dyskinesias

HP:0002310

Personality changes

HP:0000751

Repetitive behaviour Stereotypic behaviour

HP:0000733

Restlessness

HP:0000711

Urinary incontinence

HP:0000020

Related Conditions

Autosomal dominant hereditary disorder(parent)

Frontotemporal dementia(parent)

Hereditary degenerative disease of central nervous system(parent)

Quick Facts

SNOMED CT: 702393003
UMLS CUI: C1833296
Fully Specified Name: Frontotemporal dementia with gene located on 3p11 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 26

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.