Term Name: spondylocostal dysostosis 3
Synonyms: autosomal recessive spondylocostal dysostosis 3, SCDO3
Definition: A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the LFNG gene on chromosome 7p22.3.
Ontology: Human Disease [DOID:0112361]   ( DOID:0112361 )

Relationships
is a type of: autosomal recessive disease spondylocostal dysostosis