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Human Disease

spondylocostal dysostosis 2

Term ID
DOID:0112362
Synonyms
  • autosomal recessive spondylocostal dysostosis 2
  • SCDO2
Definition
A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the MESP2 gene on chromosome 15q26.1. https://pubmed.ncbi.nlm.nih.gov/15122512/
References
Ontology
Human Disease   ( DOID:0112362 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models