_:vb50942198 . _:vb50942198 "A bone development disease that is characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the Wnt family member 7A (WNT7A) gene on chromosome 3p25."^^ . _:vb50942198 "url:https://www.omim.org/entry/228930"^^ . _:vb50942198 . _:vb50942198 . _:vb50942198 . _:vb50942198 . _:vb50942198 . _:vb50942198 "url:https://www.ncbi.nlm.nih.gov/pubmed/28917830"^^ .