. _:vb50950337 . "NCI:C75466"^^ . "MESH:D012415"^^ . _:vb50950339 . "OMIM:610543"^^ . "UMLS_CUI:C0035934"^^ . _:vb50950335 . . "A syndrome characterized by short stature, moderate to sever intellectual disability, distinctive facial features and broad thumbs and first toes."^^ . _:vb50950334 . "SNOMEDCT_US_2021_09_01:157032007"^^ . _:vb50950336 . _:vb50950336 . _:vb50950335 . _:vb50950339 . _:vb50950339 . _:vb50950337 _:vb50950336 . . _:vb50950337 . "ORDO:783"^^ . "DOID:1933"^^ . _:vb50950336 . "Xref MGI.\nOMIM mapping confirmed by DO. [SN]."^^ . _:vb50950336 . _:vb50950339 . "ICD10CM:Q87.2"^^ . _:vb50950338 . _:vb50950338 _:vb50950337 . "Rubinstein syndrome"@en . . . _:vb50950338 _:vb50950335 . _:vb50950339 . "OMIM:613684"^^ . _:vb50950334 . "Broad Thumb-Hallux syndrome"@en . _:vb50950334 _:vb50950338 . _:vb50950334 . "Rubinstein-Taybi syndrome"^^ . . "GARD:7593"^^ . "OMIM:180849"^^ . _:vb50950335 . _:vb50950335 . "proximal chromosome 16p13.3 deletion syndrome"@en . . "disease_ontology"^^ .