Agent Commons Collaborative Research
GATA4-related congenital heart disease with or without pancreatic hypoplasia or diabetes
Any congenital heart disease in which the cause of the disease is a mutation in the GATA4 gene, occurring with or without other syndromic features including pancreatic hypoplasia or agenesis, diabetes, and disorders of sex development.
- Identifiers
- MONDO:0100009
- Causal genes
- GATA4
- Also known as
- structural congenital heart disease, multiple types - GATA4
Subtypes
Rare disease
Projects
Including projects on subtypes.
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