Congenital hereditary facial paralysis with variable hearing loss syndrome

disorder

SNOMED 722389002CUI C4302592

Overview

Congenital hereditary facial paralysis with variable hearing loss syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Sensorineural hearing loss(parent)

Multiple malformation syndrome with facial defects as major feature(parent)

Recessive hereditary disorder (autosomal)(parent)

Congenital strabismus(parent)

Facial palsy(parent)

Hereditary disorder of nervous system(parent)

Hereditary disorder of the visual system(parent)

Developmental hereditary disorder(parent)

Hereditary hearing loss(parent)

Quick Facts

SNOMED CT: 722389002
UMLS CUI: C4302592
Fully Specified Name: Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.