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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
Spondylocostal dysostosis 7, autosomal recessive
rare
Identifiers
MONDO:0981023
OMIM:621523
Causal genes
DMRT2
Part of
Spondylocostal dysostosis
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