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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 2
1 OMIM reference -
5 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Cree leukoencephalopathy

APP EIF2B1
EIF2B2
EIF2B3
EIF2B4
EIF2B5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
APP
(0.56)
(0.56)
EIF2B2
EIF2B5



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Cree leukoencephalopathy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Cree leukoencephalopathy

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

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



Cree leukoencephalopathy

(no data available)