Primary progressive non fluent aphasia

disorder

SNOMED 716281000CUI C0751706

Overview

Primary progressive non fluent aphasia is a disorder.

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

Signs & Symptoms

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

Deficit in grammar

Very frequent (80-99%)HP:0006977

Difficulty finding words

Very frequent (80-99%)HP:0002381

Frontotemporal cerebral atrophy

Very frequent (80-99%)HP:0006892

Frontotemporal dementia

Very frequent (80-99%)HP:0002145

Intellectual deterioration

Very frequent (80-99%)HP:0001268

Memory impairment

Very frequent (80-99%)HP:0002354

Spoken word recognition deficit

Very frequent (80-99%)HP:0030391

Temporal cortical atrophy

Very frequent (80-99%)HP:0007112

Thickened skin folds of neck

Very frequent (80-99%)HP:0000474

Abnormal brain FDG PET scan

Frequent (30-79%)HP:0012658

Abnormality of the cerebral white matter

Frequent (30-79%)HP:0002500

Alexia

Frequent (30-79%)HP:0010523

Anxiety disease

Frequent (30-79%)HP:0000739

Apraxia

Frequent (30-79%)HP:0002186

Depression

Frequent (30-79%)HP:0000716

EEG with continuous slow activity

Frequent (30-79%)HP:0011204

Behavioural disorders

Occasional (5-29%)HP:0000708

Dysgraphia

Occasional (5-29%)HP:0010526

Extrapyramidal dysfunction

Occasional (5-29%)HP:0002071

Increase in astrocyte number

Occasional (5-29%)HP:0002446

Lower motor neuron manifestations

Occasional (5-29%)HP:0002366

Motor aphasia

Occasional (5-29%)HP:0002427

Mutism

Occasional (5-29%)HP:0002300

Parkinsonian disease

Occasional (5-29%)HP:0001300

Perseverative behaviour

Occasional (5-29%)HP:0030223

Personality changes

Occasional (5-29%)HP:0000751

Restlessness

Occasional (5-29%)HP:0000711

Senile plaques

Occasional (5-29%)HP:0100256

Related Conditions

Progressive aphasia(parent)

Quick Facts

SNOMED CT: 716281000
UMLS CUI: C0751706
Fully Specified Name: Primary progressive non fluent aphasia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

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.