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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Mucocutaneous venous malformations

APP TEK


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Mucocutaneous venous malformations
TEK



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Mucocutaneous venous malformations

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Cutaneous and mucosal venous malformation
- VMCM

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 genetic disease

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

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

Mucocutaneous venous malformations

Very frequent
- Arteriovenous malformations / vascular malformations (excluding port-wine stains)
- Autosomal dominant inheritance
- Vascular anomalies of skin / mucosae



Hereditary cerebral hemorrhage with amyloidosis, Flemish type

(no data available)