. _:vb50939114 . . _:vb50939114 . "OMIM:302350"^^ . "UMLS_CUI:C0796085"^^ . "GARD:7161"^^ . "A syndrome that has_material_basis_in mutation in the NHS gene on chromosome Xp22 and is characterized by congenital cataract leading to profound vision loss, characteristic dysmorphic features and dental anomalies."^^ . _:vb50939114 . "SNOMEDCT_US_2021_09_01:445257004"^^ . "ORDO:627"^^ . . "MESH:C538336"^^ . _:vb50939114 . "disease_ontology"^^ . "DOID:0060599"^^ . . _:vb50939114 . "Nance-Horan syndrome"^^ .