_:vb50942090 . "ORDO:71271"^^ . . "disease_ontology"^^ . "A split-hand/foot malformation characterized by split-hand/foot malformation and sensorineural hearing impairment that has_material_basis_in homozygous mutation in the DLX5 gene on chromosome 7q21."^^ . _:vb50942092 . _:vb50942088 . "ICD10CM:Q87.2"^^ . _:vb50942089 _:vb50942090 . "DOID:0090024"^^ . _:vb50942090 . "OMIM:220600"^^ . _:vb50942088 . . _:vb50942089 . _:vb50942089 . _:vb50942090 _:vb50942092 . . _:vb50942092 . _:vb50942089 . _:vb50942088 . _:vb50942091 . "SHFM1D"@en . _:vb50942088 . . _:vb50942089 . "split hand-foot malformation 1 with sensorineural hearing loss"^^ . _:vb50942088 . _:vb50942092 _:vb50942091 . _:vb50942091 . "congenital deafness with split hands and feet"@en . _:vb50942091 .