has material basis in germline mutation in TNNT1 nemaline myopathy 5 https://www.malacards.org/card/nemaline_myopathy_5a https://www.malacards.org/card/nemaline_myopathy_5a_autosomal_recessive_severe_infantile MONDO:0011539 UMLS:C1854380 ANM GARD:0008334 nemaline myopathy, caused by mutation in the troponin t1 gene MEDGEN:344273 TNNT1 nemaline myopathy nemaline myopathy caused by mutation in TNNT1 Orphanet:98902 NEM5 Amish nemaline myopathy is a type of nemaline myopathy (NM) only observed in several families of the Amish community. nemaline myopathy type 5 nemaline myopathy 5 Amish nemaline myopathy OMIM:605355 MESH:C538397 DOID:0110936 nemaline myopathy