ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Familial isolated congenital asplenia

Complete atrioventricular canal - left heart obstruction

NKX2-5	(UniProt - OMIM)		CRELD1	(UniProt - OMIM)
RPSA	(UniProt - OMIM)		GATA4	(UniProt - OMIM)


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

Citations in the biomedical literature:

Familial isolated congenital asplenia		Complete atrioventricular canal - left heart obstruction
	Synonym(s): (no synonyms)		Synonym(s): - CAVC - left heart obstruction - CAVC type A - Complete atrioventricular canal type A

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - 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: (no data available)

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

No signs/symptoms info available.