congenital structural myopathy nemaline myopathy https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/nemaline_myopathy MEDGEN:61528 NANDO:1200478 congenital rod disease nemaline myopathy SCTID:75072002 Orphanet:607 nemaline rod disease NANDO:2200869 NEM DOID:3191 OMIMPS:256030 Rod-body myopathy MONDO:0018958 MESH:D017696 nemaline body disease UMLS:C0206157 nemaline rod myopathy NM Nemaline myopathy (NM) encompasses a large spectrum of myopathies characterized by hypotonia, weakness and depressed or absent deep tendon reflexes, with pathologic evidence of nemaline bodies (rods) on muscle biopsy. icd11.foundation:1996502540 GARD:0012033 Rod body disease rod myopathy ICD10CM:G71.21