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Atrial septal defect, ostium secundum type
8 OMIM references -
8 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Benign familial chorea
2 OMIM references -
1 associated gene
2 signs/symptoms
Atrial septal defect, ostium secundum type
Benign familial chorea

ACTC1
(UniProt - OMIM)
 NKX2-1
(UniProt - OMIM)
CITED2
(UniProt - OMIM)
GATA4
(UniProt - OMIM)
GATA6
(UniProt - OMIM)
MYH6
(UniProt - OMIM)
NKX2-5
(UniProt - OMIM)
TBX20
(UniProt - OMIM)
TLL1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GATA6
(0.72)
NKX2-1


Citations in the biomedical literature:


Atrial septal defect, ostium secundum type
ACTC1 CITED2 GATA4 GATA6 MYH6 NKX2-5
TBX20 TLL1
Benign familial chorea
NKX2-1



Atrial septal defect, ostium secundum type
Benign familial chorea

Synonym(s):
- ASD, ostium secundum type
Synonym(s):
- Hereditary benign chorea
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
8 OMIM references -
No MeSH references
External references:
2 OMIM references -
No MeSH references
Benign familial chorea

Very frequent
- Abnormal gait
- Movement disorder



Atrial septal defect, ostium secundum type

(no data available)