Wildervanck's syndrome

disorder

SNOMED 79665007CUI C0265239

Overview

Wildervanck's syndrome 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.

Abducens nerve paralysis

Very frequent (80-99%)HP:0006897

Bilateral congenital sensorineural deafness

Very frequent (80-99%)HP:0008527

Fused neck

Very frequent (80-99%)HP:0002949

Short neck

Very frequent (80-99%)HP:0000470

Facial muscle weakness of muscles innervated by CN VII

Occasional (5-29%)HP:0010628

Low posterior hair line

Occasional (5-29%)HP:0002162

Meningocele

Occasional (5-29%)HP:0002435

Partially dislocated lens

Occasional (5-29%)HP:0001132

Pseudopapilledema

Occasional (5-29%)HP:0000538

Pterygium colli

Occasional (5-29%)HP:0000465

Unbalanced face

Occasional (5-29%)HP:0000324

Ear anomalies

HP:0000356

Hearing impairment

HP:0000365

Preauricular skin tags

HP:0000384

Related Conditions

Duane's syndrome(parent)

Klippel-Feil sequence(parent)

Congenital sensorineural hearing loss(parent)

Quick Facts

SNOMED CT: 79665007
UMLS CUI: C0265239
Fully Specified Name: Wildervanck syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.