ODCs

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

PROTEIN INTERACTIONS: 1

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

Chilblain lupus

Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

SAMHD1	(UniProt - OMIM)		ATR	(UniProt - OMIM)
TREX1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TREX1	(0.55)	ATR

Citations in the biomedical literature:

Chilblain lupus		Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

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

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.