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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Spondylocostal dysostosis
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Autosomal recessive spondylocostal dysostosis
Spondylocostal dysostosis 2, autosomal recessive
rare
Identifiers
MONDO:0012097
OMIM:608681
Causal genes
MESP2
Part of
Autosomal recessive spondylocostal dysostosis
Also known as
SCDO2 · spondylocostal dysostosis 2
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