Term Name: autosomal dominant craniodiaphyseal dysplasia
Synonyms:
Definition: A craniodiaphyseal dysplasia that has_material_basis_in heterozygous mutation in the SOST gene on chromosome 17q21.
Ontology: Human Disease [DOID:0080807]   ( DOID:0080807 )

Relationships
is a type of: autosomal dominant disease craniodiaphyseal dysplasia