ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

MÃ©niÃ¨re disease

Autosomal dominant rhegmatogenous retinal detachment


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COCH	(0.72)	COL2A1

Citations in the biomedical literature:

MÃ©niÃ¨re disease		Autosomal dominant rhegmatogenous retinal detachment

	Classification (Orphanet): - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare eye disease - Rare genetic 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: adulthood Average age of death: - 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.