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Ménière disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Ehlers-Danlos syndrome, vascular-like type
1 associated gene
No signs/symptoms info
Ménière disease
Ehlers-Danlos syndrome, vascular-like type

COCH
(UniProt - OMIM)
 COL1A1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
COCH
(0.72)
COL1A1


Citations in the biomedical literature:


Ménière disease
COCH
Ehlers-Danlos syndrome, vascular-like type
COL1A1



Ménière disease
Ehlers-Danlos syndrome, vascular-like type

Synonym(s):
(no synonyms)

Synonym(s):
- EDS, vascular-like type
Classification (Orphanet):
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the ear and mastoid process -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D008575
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.