Paroxysmal kinesigenic choreoathetosis

disorder

SNOMED 609221008CUI C1868682

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.

Episodic dystonia

Always present (100%)HP:0002268

Athetoid movements

Very frequent (80-99%)HP:0002305

Choreiform movements

Very frequent (80-99%)HP:0002072

Dyskinesia

Very frequent (80-99%)HP:0100660

Dystonic disease

Very frequent (80-99%)HP:0001332

Involuntary movements

Very frequent (80-99%)HP:0004305

Focal sensory seizures

Frequent (30-79%)HP:0011157

Infantile spasms

Occasional (5-29%)HP:0012469

Migraine headache

Occasional (5-29%)HP:0002076

Seizures

Occasional (5-29%)HP:0001250

Writer's cramp

Occasional (5-29%)HP:0002356

Choreoathetosis, episodic

HP:0007098

Orofacial dyskinesias

HP:0002310

Related Conditions

Infantile convulsion and choreoathetosis syndrome(child)

Paroxysmal choreoathetosis(parent)

Quick Facts

SNOMED CT: 609221008
UMLS CUI: C1868682
Fully Specified Name: Paroxysmal kinesigenic dyskinesia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.