. . "NEM7"@en . "disease_ontology"^^ . _:vb50943945 . . "A nemaline myopathy characterized by very early onset of hypotonia and delayed motor development that has_material_basis_in homozygous mutation in the CFL2 gene on chromosome 14q13."^^ . _:vb50943945 . _:vb50943945 . "DOID:0110934"^^ . _:vb50943945 . "OMIM:610687"^^ . . "nemaline myopathy 7"^^ . _:vb50943945 . "nemaline myopathy 7, autosomal recessive"@en .