Cytoscape Web
Click node...

Ménière disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
1 OMIM reference -
1 associated gene
No signs/symptoms info
Ménière disease
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures

COCH
(UniProt - OMIM)
 COL4A1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
COCH
(0.72)
COL4A1


Citations in the biomedical literature:


Ménière disease
COCH
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
COL4A1



Ménière disease
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures

Synonym(s):
(no synonyms)

Synonym(s):
- HANAC syndrome
- Hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome
Classification (Orphanet):
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the ear and mastoid process -
Classification (ICD10):
- Diseases of the eye and adnexa -
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: childhood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D008575
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.