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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

NF1 APP


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

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

Synonym(s):
- HCHWA, Flemish type

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

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

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

No signs/symptoms info available.