Infantile-onset generalised dyskinesia with orofacial involvement

disorder

SNOMED 1172603005CUI C5567464

Overview

Infantile-onset generalised dyskinesia with orofacial involvement 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

Frequent (30-79%)HP:0002072

Difficulty articulating speech

Frequent (30-79%)HP:0001260

Drooling

Frequent (30-79%)HP:0002307

Feeding difficulties

Frequent (30-79%)HP:0011968

Nasogastric tube feeding in infancy

Frequent (30-79%)HP:0011470

Truncal hypotonia

Frequent (30-79%)HP:0008936

Unsteady walk

Frequent (30-79%)HP:0002317

Hemiballismus

Occasional (5-29%)HP:0100248

Tremor

Occasional (5-29%)HP:0001337

Delayed motor milestones

HP:0001270

Dyskinesia

HP:0100660

Epilepsy

HP:0001250

Frequent falls

HP:0002359

Hyperkinetic movements

HP:0002487

Orofacial dyskinesias

HP:0002310

Related Conditions

Dystonia(parent)

Hereditary disorder of nervous system(parent)

Orofacial dyskinesia(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1172603005
UMLS CUI: C5567464
Fully Specified Name: Infantile-onset generalized dyskinesia with orofacial involvement (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.