. "NCI:C98670"^^ . "GARD:7883"^^ . _:vb50948747 . "ICD9CM:335.0"^^ . "A childhood spinal muscular atrophy that is a severe form and is characterized by muscle weakness onset from birth to six months of age, the inability to sit unassisted."^^ . "ICD10CM:G12.0"^^ . _:vb50948747 . _:vb50948746 . . "HMN (Hereditary motor Neuropathy) Proximal type I"@en . "OMIM mapping confirmed by DO. [SN]."^^ . _:vb50948747 . "SMA1"@en . "SNOMEDCT_US_2021_09_01:64383006"^^ . "OMIM:253300"^^ . _:vb50948746 . _:vb50948746 . _:vb50948747 . "Spinal muscular atrophy 1"@en . "MESH:D014897"^^ . _:vb50948746 . "disease_ontology"^^ . . _:vb50948747 . "Werdnig-Hoffmann disease"^^ . "DOID:13137"^^ . "progressive muscular atrophy of infancy"@en . "hereditary motor neuropathy proximal type I"@en . _:vb50948746 . "infantile muscular atrophy"@en . . "UMLS_CUI:C0043116"^^ .