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Chilblain lupus

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

COMMON GENES: 1

Hereditary vascular retinopathy

1 OMIM reference -
1 associated gene
3 signs/symptoms

Chilblain lupus

Hereditary vascular retinopathy

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


COMMON GENES	TREX1

Citations in the biomedical literature:

Chilblain lupus		Hereditary vascular retinopathy
	Synonym(s): (no synonyms)		Synonym(s): - HVR - Hereditary vascular retinopathy - Raynaud phenomenon - migraine

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic 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: adulthood Average age of death: no data available Type of inheritance: autosomal dominant

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

Hereditary vascular retinopathy
	Very frequent - Anomalies of eyes and vision - Autosomal dominant inheritance - Visual loss / blindness / amblyopia
Chilblain lupus
(no data available)