ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Chilblain lupus

Congenital myopathy, Paradas type

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


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

Citations in the biomedical literature:

Chilblain lupus		Congenital myopathy, Paradas type

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

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

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

	External references: 2 OMIM references - 1 MeSH reference: C535924		External references: No OMIM references No MeSH references

No signs/symptoms info available.