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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
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion

APP NF1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.73)
NF1



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion
NF1



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Von Recklinghausen disease due to NF1 mutation or intragenic deletion

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare skin disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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



Neurofibromatosis type 1 due to NF1mutation or intragenic deletion

(no data available)