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Ménière disease
1 OMIM reference -
1 associated gene
35 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Achondrogenesis type 2
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Autosomal dominant rhegmatogenous retinal detachment
Caffey disease
Czech dysplasia, metatarsal type
Dermatofibrosarcoma protuberans
Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, vascular-like type
Ehlers-Danlos / osteogenesis imperfecta syndrome
Familial avascular necrosis of femoral head
Familial porencephaly
Familial vascular leukoencephalopathy
High bone mass osteogenesis imperfecta
Kniest dysplasia
Legg-Calvé-Perthes disease
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis
Multiple epiphyseal dysplasia, Beighton type
Osteogenesis imperfecta type 1
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Otospondylomegaepiphyseal dysplasia
Platyspondylic dysplasia, Torrance type
Spondyloepimetaphyseal dysplasia congenita, Strudwick type
Spondyloepiphyseal dysplasia congenita
Spondylometaphyseal dysplasia, 'corner fracture' type
Spondylometaphyseal dysplasia, Schmidt type
Spondyloperipheral dysplasia - short ulna
Stickler syndrome type 1
Walker-Warburg syndrome
(no synonyms)

Classification (Orphanet):
- Rare otorhinolaryngologic disease

Classification (ICD10):
- Diseases of the ear and mastoid process -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
1 MeSH reference: D008575

Gene symbol UniProt reference OMIM reference
COCH O43405603196
No signs/symptoms info available.