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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
8 OMIM references -
8 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Atrial septal defect, ostium secundum type

APP ACTC1
CITED2
GATA4
GATA6
MYH6
NKX2-5
TBX20
TLL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
TLL1



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Atrial septal defect, ostium secundum type
ACTC1 CITED2 GATA4 GATA6 MYH6 NKX2-5
TBX20 TLL1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Atrial septal defect, ostium secundum type

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- ASD, ostium secundum type

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac 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:
8 OMIM references -
No MeSH references

No signs/symptoms info available.