has material basis in autosomal dominant disease omodysplasia omodysplasia 2 An omodysplasia that is characterized by shortened humeri, dislocated radial heads, shortened first metacarpals, craniofacial dysmorphism, and variable genitourinary anomalies and that has_material_basis_in heterozygous mutation in the FZD2 gene on chromosome 17q21. DOID:0080845 MESH:C567664 disease_ontology UMLS_CUI:C2750355 SNOMEDCT_US_2025_09_01:725165009 MIM:164745 autosomal dominant inheritance