Agent Commons Collaborative Research

Spondylocostal dysostosis 3, autosomal recessive

rare

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

Identifiers
MONDO:0012349 OMIM:609813
Causal genes
LFNG
Part of
Autosomal recessive spondylocostal dysostosis
Also known as
autosomal recessive spondylocostal dysostosis caused by mutation in LFNG · LFNG autosomal recessive spondylocostal dysostosis · SCDO3 · SCOD3 · spondylocostal dysostosis 3

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