Familial Alzheimer-like prion disease

disorder

SNOMED 721219005CUI C4303482

Overview

Familial Alzheimer-like prion disease 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.

Abdominal symptom

Very frequent (80-99%)HP:0011458

Behavioral changes

Very frequent (80-99%)HP:0000708

Childhood attention deficit/hyperactivity disorder

Very frequent (80-99%)HP:0007018

Deficit in non-word repetition

Very frequent (80-99%)HP:0002549

Depression

Very frequent (80-99%)HP:0000716

Emotional lability

Very frequent (80-99%)HP:0000712

Excessive, persistent worry and fear

Very frequent (80-99%)HP:0000739

Intellectual impairment

Very frequent (80-99%)HP:0100543

Jaw pain

Very frequent (80-99%)HP:0040264

Perseverative behaviour

Very frequent (80-99%)HP:0030223

Specific learning disability

Very frequent (80-99%)HP:0001328

Trouble sleeping

Very frequent (80-99%)HP:0002360

Related Conditions

Autosomal dominant hereditary disorder(parent)

Prion disease(parent)

Familial disease(parent)

Hereditary degenerative disease of central nervous system(parent)

Quick Facts

SNOMED CT: 721219005
UMLS CUI: C4303482
Fully Specified Name: Familial Alzheimer-like prion disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.