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

Von Willebrand disease type 3

Spinocerebellar ataxia type 7


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VWF	(0.63)	ATXN7

Citations in the biomedical literature:

Von Willebrand disease type 3		Spinocerebellar ataxia type 7
	Synonym(s): - Willebrand disease type 3		Synonym(s): - Autosomal dominant spinocerebellar ataxia type 7 - Cerebellar syndrome - pigmentary maculopathy - SCA7

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D056729		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.