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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
2 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Syndactyly type 8

APP FGF16


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
FGF16



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Syndactyly type 8
FGF16



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Syndactyly type 8

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Fusion of metacarpals 4 and 5

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare bone 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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

Syndactyly type 8

Very frequent
- Metacarpal anomalies / Archibald's sign
- X-linked recessive inheritance



Hereditary cerebral hemorrhage with amyloidosis, Flemish type

(no data available)