Autosomal dominant focal dystonia DYT25 type

disorder

SNOMED 719516000CUI C4304670

Overview

Autosomal dominant focal dystonia DYT25 type 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.

Focal dystonia

Very frequent (80-99%)HP:0004373

Abnormal craniofacial muscle tone

Frequent (30-79%)HP:0012179

Axial dystonia

Frequent (30-79%)HP:0002530

Limb dystonia

Frequent (30-79%)HP:0002451

Spasmodic dysphonia

Frequent (30-79%)HP:0012049

Spasmodic torticollis

Frequent (30-79%)HP:0000473

Tongue dystonia

Frequent (30-79%)HP:0031008

Dysphonia

HP:0001618

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Focal dystonia(parent)

Quick Facts

SNOMED CT: 719516000
UMLS CUI: C4304670
Fully Specified Name: Autosomal dominant focal dystonia DYT25 type (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.