has material basis in germline mutation in TPM3 congenital myopathy 4B, autosomal recessive https://www.malacards.org/card/congenital_myopathy_4b_autosomal_recessive UMLS:C5829889 Any congenital myopathy in which the cause of the disease is a mutation in the TPM3 gene. DOID:0110926 TPM3 nemaline myopathy MESH:C538348 OMIM:609284 nemaline myopathy caused by mutation in TPM3 GARD:0015453 nemaline myopathy 1 nemaline myopathy type 1 MONDO:0012239 MEDGEN:1840525 NEM1 Nem1 intermediate nemaline myopathy childhood-onset nemaline myopathy nemaline myopathy TPM3-related myopathy