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Ménière disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Osteogenesis imperfecta type 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Ménière disease
Osteogenesis imperfecta type 1

COCH
(UniProt - OMIM)
 COL1A1
(UniProt - OMIM)
COL1A2
(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
Osteogenesis imperfecta type 1
COL1A1 COL1A2



Ménière disease
Osteogenesis imperfecta type 1

Synonym(s):
(no synonyms)

Synonym(s):
- Adair-Dighton syndrome
- Mild osteogenesis imperfecta
- Non-deforming osteogenesis imperfecta
- OI type 1
- Van der Hoeve syndrome
Classification (Orphanet):
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic 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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D008575
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.