ODCs

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

PROTEIN INTERACTIONS: 1

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

Congenital myopathy with excess of thin filaments

Autoimmune lymphoproliferative syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.55)	PRKCD

Citations in the biomedical literature:

Congenital myopathy with excess of thin filaments		Autoimmune lymphoproliferative syndrome
	Synonym(s): - Actin myopathy		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: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.