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2 OMIM references -
3 associated genes
17 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
BOR syndrome
Sensorineural deafness with dilated cardiomyopathy

EYA1 EYA4
SIX1
SIX5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SIX1
(0.74)
EYA4



Citations in the biomedical literature:


BOR syndrome
EYA1 SIX1 SIX5
Sensorineural deafness with dilated cardiomyopathy
EYA4



BOR syndrome
Sensorineural deafness with dilated cardiomyopathy

Synonym(s):
- Branchiootorenal syndrome

Synonym(s):
- Neurosensory deafness with dilated cardiomyopathy
- Neurosensory hearing loss with dilated cardiomyopathy
- Sensorineural hearing loss with dilated cardiomyopathy

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare otorhinolaryngologic disease
- Rare renal disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
1 MeSH reference: D019280
External references:
1 OMIM reference -
No MeSH references

BOR syndrome

Very frequent
- Autosomal dominant inheritance
- Hearing loss / hypoacusia / deafness

Frequent
- Agenesis / hypoplasia / aplasia of kidneys
- Branchial / posterior auricular / preauricular / cheek cysts / fistulae
- External ear anomalies
- Preauricular / branchial tags / appendages
- Structural anomalies of inner ear / cochlea / vestible / semicircular canals
- Structural anomalies of middle ear / ossicles / tympanic cavity

Occasional
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Defect / anomaly of lacrimal system
- External auditory canal atresia / stenosis / agenesis
- Facial palsy
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Micrognathia / retrognathia / micrognathism / retrognathism
- Multicystic kidney / renal dysplasia
- Renal failure
- Vesicorenal / vesicoureteral reflux


Sensorineural deafness with dilated cardiomyopathy

(no data available)