Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
10 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Cerebroretinal vasculopathy
Hereditary combined deficiency of vitamin K-dependent clotting factors

TREX1 GGCX
VKORC1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Cerebroretinal vasculopathy
TREX1
Hereditary combined deficiency of vitamin K-dependent clotting factors
GGCX VKORC1



Cerebroretinal vasculopathy
Hereditary combined deficiency of vitamin K-dependent clotting factors

Synonym(s):
- CRV
- Grand-Kaine-Fulling syndrome

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: -
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

Cerebroretinal vasculopathy

Very frequent
- Autosomal dominant inheritance
- Mild visual loss / impaired visual acuity
- Retinal vascular anomalies / retinal telangiectasia
- Structural anomalies of the nervous system

Frequent
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia

Occasional
- Cataract / lens opacification
- Glaucoma
- Seizures / epilepsy / absences / spasms / status epilepticus
- Visual loss / blindness / amblyopia


Hereditary combined deficiency of vitamin K-dependent clotting factors

(no data available)