Spondylocostal dysostosis 3, autosomal recessive

MONDO:0012349

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

Also known as: LFNG autosomal recessive spondylocostal dysostosis, autosomal recessive spondylocostal dysostosis caused by mutation in LFNG, spondylocostal dysostosis 3, autosomal recessive, SCDO3, SCOD3, spondylocostal dysostosis 3

17 clinical trials for this condition and its sub-types, 0 tagged with Spondylocostal dysostosis 3, autosomal recessive itself.

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↑ Autosomal recessive spondylocostal dysostosis (0)

Including sub-types (17) Tagged with Spondylocostal dysostosis 3, autosomal recessive (0)

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