Term Name: spondylocostal dysostosis 2
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.
Ontology: Human Disease [DOID:0112362]   ( DOID:0112362 )

Relationships
is a type of: autosomal recessive disease spondylocostal dysostosis