Benign hereditary chorea

disorder

SNOMED 230306001CUI C0393584

Overview

Benign hereditary chorea 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.

Choreiform movements

Always present (100%)HP:0002072

No development of motor milestones

Always present (100%)HP:0001270

Abnormality of movement

Very frequent (80-99%)HP:0100022

Gait disturbance

Very frequent (80-99%)HP:0001288

Difficulty articulating speech

Occasional (5-29%)HP:0001260

Frequent falls

Occasional (5-29%)HP:0002359

Anxiety disease

HP:0000739

Progressive dementia

Excluded (<1%)HP:0000726

Related Conditions

Childhood-onset benign chorea with striatal involvement(child)

Hereditary disorder of nervous system(parent)

Chorea(parent)

Quick Facts

SNOMED CT: 230306001
UMLS CUI: C0393584
Fully Specified Name: Benign hereditary chorea (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.