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Branchio-otic syndrome

disorder
SNOMED 764810000CUI C4273131

Overview

Branchio-otic 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.

Hearing impairment
Very frequent (80-99%)HP:0000365
Preauricular earpits
Very frequent (80-99%)HP:0004467
Abnormal middle ear morphology
Frequent (30-79%)HP:0008609
Abnormality of the auricle
Frequent (30-79%)HP:0000356
Absent external auditory canals
Frequent (30-79%)HP:0000413
Branchial cleft fistula
Frequent (30-79%)HP:0009795
Hearing loss, conductive
Frequent (30-79%)HP:0000405
Inner ear abnormality
Frequent (30-79%)HP:0000359
Sensorineural deafness
Frequent (30-79%)HP:0000407
Abnormal nasolacrimal system morphology
Occasional (5-29%)HP:0000614
Cleft of palate
Occasional (5-29%)HP:0000175
Facial palsy
Occasional (5-29%)HP:0010628
Hypoplastic mandible
Occasional (5-29%)HP:0000347
Lip pit
Occasional (5-29%)HP:0100267
Preauricular skin tags
Occasional (5-29%)HP:0000384
Unbalanced face
Occasional (5-29%)HP:0000324
Capuchin ears
HP:0000378
Cochlear malformation
HP:0008554
Enlarged internal auditory canal
HP:0004458
Hearing loss, mixed
HP:0000410
Hypoplastic cochlea
HP:0008586
Low-set ears
HP:0000369
Microtia
HP:0008551
Retrognathia
HP:0000278

Quick Facts

SNOMED CT
764810000
UMLS CUI
C4273131
Fully Specified Name
Branchiootic syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
24
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.