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1 OMIM reference -
1 associated gene
9 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
13 signs/symptoms
Coats disease
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type

NDP APP


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



Coats disease
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type

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

Synonym(s):
- HCHWA, Piedmont type

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

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

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

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

Coats disease
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type

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


Very frequent
- Autosomal dominant inheritance
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Intracranial / cerebral / meningeal hemorrhage
- Motor deficit / trouble
- Obnubilation / coma / lethargia / desorientation
- Paresthesia / dysesthesia / hypoesthesia / anesthesia / numbness
- Psychic / psychomotor regression / dementia / intellectual decline
- Sensitive trouble / deficit
- Transient cerebral ischemia / stroke

Frequent
- Cerebral vascular anomalies
- Facial pain / cephalalgia / migraine
- Psychic / behavioural troubles

Occasional
- Early death / lethality