"ICD9CM:759.83"^^ . . . . "MESH:D005600"^^ . "OMIM mapping confirmed by DO. [SN]."^^ . "ORDO:908"^^ . "OMIM:300624"^^ . "fragile X syndrome"^^ . _:vb50949515 . "MARKER X SYNDROME"@en . "GARD:6464"^^ . "DOID:14261"^^ . . "FRAGILE X MENTAL RETARDATION SYNDROME"@en . "ICD10CM:Q99.2"^^ . "SNOMEDCT_US_2021_09_01:390007001"^^ . _:vb50949515 . _:vb50949515 . "NCI:C84717"^^ . "disease_ontology"^^ . "UMLS_CUI:C0016667"^^ . "A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function."^^ . _:vb50949515 . . "MARTIN-BELL SYNDROME"@en . . _:vb50949515 .