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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
9 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Coats disease

APP NDP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
NDP



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Coats disease
NDP



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Coats disease

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Congenital retinal telangiectasia
- Leber miliary aneurysm

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the eye and adnexa -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D058456

Coats disease

Very frequent
- Retinal vascular anomalies / retinal telangiectasia
- Strabismus / squint

Frequent
- Glaucoma
- Macular dystrophy / absence / hypoplasia of the macula
- Retinal detachment

Occasional
- Aniridia / iris hypoplasia
- Anterior chamber anomaly
- Cataract / lens opacification
- Visual loss / blindness / amblyopia


Hereditary cerebral hemorrhage with amyloidosis, Flemish type

(no data available)