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8 OMIM references -
8 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Atrial septal defect, ostium secundum type
Atrial septal defect - atrioventricular conduction defects

ACTC1 NKX2-5
CITED2
GATA4
GATA6
MYH6
NKX2-5
TBX20
TLL1


COMMON
GENES
NKX2-5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GATA4
(0.96)
NKX2-5



Citations in the biomedical literature:


Atrial septal defect, ostium secundum type
ACTC1 CITED2 GATA4 GATA6 MYH6 NKX2-5
TBX20 TLL1
Atrial septal defect - atrioventricular conduction defects



Atrial septal defect, ostium secundum type
Atrial septal defect - atrioventricular conduction defects

Synonym(s):
- ASD, ostium secundum type

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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: no data available
Average age of death: no data available
Type of inheritance: autosomal dominant

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

Atrial septal defect - atrioventricular conduction defects

Very frequent
- Autosomal dominant inheritance
- Cardiac conduction defect / sinoauricular / heart / auriculoventricular / branch block
- Cardiac septal defect



Atrial septal defect, ostium secundum type

(no data available)