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Pancreatic hypoplasia - diabetes - congenital heart disease
1 OMIM reference -
1 associated gene
1 sign/symptom
COMMON GENES: 1
Atrial septal defect, ostium secundum type
8 OMIM references -
8 associated genes
No signs/symptoms info
Pancreatic hypoplasia - diabetes - congenital heart disease
Atrial septal defect, ostium secundum type

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

COMMON
GENES 		GATA6


Citations in the biomedical literature:


Pancreatic hypoplasia - diabetes - congenital heart disease
GATA6
Atrial septal defect, ostium secundum type
ACTC1 CITED2 GATA4 MYH6 NKX2-5
TBX20 TLL1



Pancreatic hypoplasia - diabetes - congenital heart disease
Atrial septal defect, ostium secundum type

Synonym(s):
- Yorifuji-Okuno syndrome
Synonym(s):
- ASD, ostium secundum type
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic 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:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
8 OMIM references -
No MeSH references
Pancreatic hypoplasia - diabetes - congenital heart disease

Very frequent
- Stillbirth / neonatal death



Atrial septal defect, ostium secundum type

(no data available)