ODCs

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1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Hereditary vascular retinopathy

Hereditary combined deficiency of vitamin K-dependent clotting factors

TREX1	(UniProt - OMIM)		GGCX	(UniProt - OMIM)
			VKORC1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TREX1	(0.63)	VKORC1

Citations in the biomedical literature:

Hereditary vascular retinopathy		Hereditary combined deficiency of vitamin K-dependent clotting factors
	Synonym(s): - HVR - Hereditary vascular retinopathy - Raynaud phenomenon - migraine		Synonym(s): - Hereditary combined deficiency of factors II, VII, IX and X

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

Hereditary vascular retinopathy
	Very frequent - Anomalies of eyes and vision - Autosomal dominant inheritance - Visual loss / blindness / amblyopia
Hereditary combined deficiency of vitamin K-dependent clotting factors
(no data available)