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Benson syndrome

disorder
SNOMED 715574002CUI C4275079

Overview

Benson syndrome 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.

Agnosia
Very frequent (80-99%)HP:0010524
Agraphia
Very frequent (80-99%)HP:0010526
Alexia
Very frequent (80-99%)HP:0010523
Anxiety disease
Very frequent (80-99%)HP:0000739
Ataxia
Very frequent (80-99%)HP:0001251
Confusion
Very frequent (80-99%)HP:0001289
CVI
Very frequent (80-99%)HP:0100704
Difficulty making arithmetical calculations
Very frequent (80-99%)HP:0002442
Finger agnosia
Very frequent (80-99%)HP:0010525
Oculomotor apraxia
Very frequent (80-99%)HP:0000657
Abnormality of vision
Frequent (30-79%)HP:0000504
Color vision defect, severe
Frequent (30-79%)HP:0000551
Dyslexia
Frequent (30-79%)HP:0010522
Limb apraxia
Frequent (30-79%)HP:0030217
Photophobia
Frequent (30-79%)HP:0000613
Abnormal REM sleep
Occasional (5-29%)HP:0002494
Inertia
Occasional (5-29%)HP:0030216
Language impairment
Occasional (5-29%)HP:0002463
Memory impairment
Occasional (5-29%)HP:0002354
Speech dyspraxia
Occasional (5-29%)HP:0011098
Visual hallucination
Occasional (5-29%)HP:0002367

Quick Facts

SNOMED CT
715574002
UMLS CUI
C4275079
Fully Specified Name
Posterior cortical atrophy syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
21
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.