ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Miyoshi myopathy

Chilblain lupus

ANO5	(UniProt - OMIM)		SAMHD1	(UniProt - OMIM)
DYSF	(UniProt - OMIM)		TREX1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DYSF	(0.63)	SAMHD1

Citations in the biomedical literature:

Miyoshi myopathy		Chilblain lupus

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: 3 OMIM references - 1 MeSH reference: C537480		External references: 2 OMIM references - 1 MeSH reference: C535924

No signs/symptoms info available.