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

Familial vascular leukoencephalopathy

MÃ©niÃ¨re disease


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

Citations in the biomedical literature:

Familial vascular leukoencephalopathy		MÃ©niÃ¨re disease
	Synonym(s): - Brain small vessel disease with hemorrhage - Retinal arteriolar tortuosity - infantile hemiparesis - autosomal dominant leukoencephalopathy		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare otorhinolaryngologic disease

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		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: C531642		External references: 1 OMIM reference - 1 MeSH reference: D008575

No signs/symptoms info available.