ODCs

Click node...

1 OMIM reference -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Familial isolated congenital asplenia

Atrial septal defect - atrioventricular conduction defects

NKX2-5	(UniProt - OMIM)		NKX2-5	(UniProt - OMIM)
RPSA	(UniProt - OMIM)

Citations in the biomedical literature:

Familial isolated congenital asplenia		Atrial septal defect - atrioventricular conduction defects

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune 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: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		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: 1 OMIM reference - 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
Familial isolated congenital asplenia
(no data available)