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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Autosomal dominant optic atrophy and cataract

APP OPA3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
OPA3



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Autosomal dominant optic atrophy and cataract
OPA3



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Autosomal dominant optic atrophy and cataract

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Autosomal dominant optic atrophy type 3
- OPA3, autosomal dominant

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- 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: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537128

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Autosomal dominant optic atrophy and cataract

(no data available)