Spondylocostal dysostosis 3, autosomal recessive

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

79 clinical trials for this condition and its sub-types.