← Back to Conditions

Primary dystonia type 2

disorder
SNOMED 715777007CUI C1857093

Overview

Primary dystonia type 2 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.

Torsion dystonia
Very frequent (80-99%)HP:0001304
Deglutition disorder
Frequent (30-79%)HP:0002015
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Feeding difficulties
Frequent (30-79%)HP:0011968
Gait disturbance
Frequent (30-79%)HP:0001288
Involuntary closure of eyelid
Frequent (30-79%)HP:0000643
Involuntary movements
Frequent (30-79%)HP:0004305
Limb dystonia
Frequent (30-79%)HP:0002451
Spasmodic torticollis
Frequent (30-79%)HP:0000473
Generalised dystonia
Occasional (5-29%)HP:0007325
Tremor
HP:0001337

Quick Facts

SNOMED CT
715777007
UMLS CUI
C1857093
Fully Specified Name
Primary dystonia type 2 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
11
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.