Term Name: spondyloepimetaphyseal dysplasia, Strudwick type
Synonyms:
Definition: A spondyloepimetaphyseal dysplasia that has_material_basis_in mutations in the COL2A1 gene which results_in short stature and multiple skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).
Ontology: Human Disease [DOID:0080028]   ( DOID:0080028 )

Relationships
is a type of: autosomal dominant disease spondyloepimetaphyseal dysplasia