ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Adult-onset distal myopathy due to VCP mutation

Spinocerebellar ataxia type 7


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VCP	(0.68)	ATXN7

Citations in the biomedical literature:

Adult-onset distal myopathy due to VCP mutation		Spinocerebellar ataxia type 7
	Synonym(s): (no synonyms)		Synonym(s): - Autosomal dominant spinocerebellar ataxia type 7 - Cerebellar syndrome - pigmentary maculopathy - SCA7

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.