Overview
Branchiogenic deafness 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.
Abnormal curving of the cornea or lens of the eye
Very frequent (80-99%)HP:0000483
Absent/small inner ear
Very frequent (80-99%)HP:0008774
Acro-osteolysis of distal phalanges
Very frequent (80-99%)HP:0009839
Branchial cleft fistula
Very frequent (80-99%)HP:0009795
Decreased body height
Very frequent (80-99%)HP:0004322
Distal phalangeal hypoplasia
Very frequent (80-99%)HP:0009882
Dysplastic ears
Very frequent (80-99%)HP:0000377
External auditory meatal atresia
Very frequent (80-99%)HP:0000413
Hearing loss, conductive
Very frequent (80-99%)HP:0000405
Hearing loss, mixed
Very frequent (80-99%)HP:0000410
Ossicular malformation
Very frequent (80-99%)HP:0004452
Overfolded helix
Very frequent (80-99%)HP:0000396
Preauricular fistulas
Very frequent (80-99%)HP:0004467
Sensorineural deafness
Very frequent (80-99%)HP:0000407
Skin tag on the posterior cheek
Very frequent (80-99%)HP:0000384
Squint
Very frequent (80-99%)HP:0000486
Underdeveloped tragus
Very frequent (80-99%)HP:0011272
Cleft of palate
Frequent (30-79%)HP:0000175
Reticulated skin pigmentation
Frequent (30-79%)HP:0007427
Specific learning disability
Frequent (30-79%)HP:0001328
Branchial cleft cyst
HP:0009796
Decrease in jaw opening
HP:0000211
Foot deformity
HP:0001760
Submucous cleft hard palate
HP:0000176
Quick Facts
- SNOMED CT
- 717944002
- UMLS CUI
- C1836673
- Fully Specified Name
- Branchiogenic deafness 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.