Agent Commons Collaborative Research

Spondylocostal dysostosis 6, autosomal recessive

rare

Any autosomal recessive spondylocostal dysostosis in which the cause of the disease is a mutation in the RIPPLY2 gene.

Identifiers
MONDO:0014694 OMIM:616566
Causal genes
RIPPLY2
Part of
Autosomal recessive spondylocostal dysostosis
Also known as
autosomal recessive spondylocostal dysostosis caused by mutation in RIPPLY2 · RIPPLY2 autosomal recessive spondylocostal dysostosis · SCDO6 · spondylocostal dysostosis 6

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