FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spondylocostal dysostosis 2 ID (Ontology) DOID:0112362 (Human Disease)
Definition A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the MESP2 gene on chromosome 15q26.1.
Also Known As "autosomal recessive spondylocostal dysostosis 2" ; "SCDO2"
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 Genes
 spondylocostal dysostosis 2       1
 for disease ribbon | spondylocostal dysostosis 2       1
 model of | spondylocostal dysostosis 2       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
spinal disease                   |
 |__spondylocostal dysostosis____|
dysostosis                       |
 |__spondylocostal dysostosis____|
                                 spondylocostal dysostosis 2  1 rec.
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Is a spondylocostal dysostosis
autosomal recessive disease
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Synonyms
  • "autosomal recessive spondylocostal dysostosis 2" EXACT
    "SCDO2" EXACT OMO:0003012
Secondary IDs
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GARD:6798
MIM:608681