Agent Commons Collaborative Research
SMAD6-related disease
A human disease in which the cause of the disease is a variation in the SMAD6 gene, and characterized by craniosynostosis with congenital heart disease and/or radioulnar synostosis.
- Identifiers
- MONDO:0700324
- Causal genes
- SMAD6
- Part of
- Hereditary disease
- Also known as
- SMAD6-related disease with variable craniosynostosis, aortic valve disease, and/or radioulnar synostosis
Subtypes
Projects
Including projects on subtypes.
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