Cytoscape Web
Click node...


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

ACTC1 APP
CITED2
GATA4
GATA6
MYH6
NKX2-5
TBX20
TLL1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

Synonym(s):
- ASD, ostium secundum type

Synonym(s):
- HCHWA, Italian type

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac 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:
8 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Hereditary cerebral hemorrhage with amyloidosis, Italian type

Very frequent
- Autosomal dominant inheritance
- Facial pain / cephalalgia / migraine
- Intracranial / cerebral / meningeal hemorrhage
- Transient cerebral ischemia / stroke

Frequent
- Obnubilation / coma / lethargia / desorientation
- Psychic / psychomotor regression / dementia / intellectual decline
- Seizures / epilepsy / absences / spasms / status epilepticus



Atrial septal defect, ostium secundum type

(no data available)