ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 OMIM references -
5 associated genes
No signs/symptoms info

Adult-onset distal myopathy due to VCP mutation

Autoimmune lymphoproliferative syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VCP	(0.56)	PRKCD

Citations in the biomedical literature:

Adult-onset distal myopathy due to VCP mutation		Autoimmune lymphoproliferative syndrome
	Synonym(s): (no synonyms)		Synonym(s): - ALPS - Canale-Smith syndrome - FAS deficiency

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare immune disease - Rare oncologic disease

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

	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: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - 1 MeSH reference: D056735

No signs/symptoms info available.