Muscular Disease,Childhood-Onset Nemaline Myopathy,Congenital Fiber-Type Disproportion,Congenital Structural Myopathy,Myopathy,Myofibrillar Myopathy,Congenital Nemaline Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Bethlem Myopathy 1,Distal Nebulin Myopathy,Myositis,Myopathy, Myofibrillar, 1,Nemaline Myopathy 3,Muscular Dystrophy,Tibial Muscular Dystrophy,Hyaline Body Myopathy,Reducing Body Myopathy,Severe Congenital Nemaline Myopathy,Intermediate Congenital Nemaline Myopathy,Typical Congenital Nemaline Myopathy,Nemaline Myopathy,Myopathy, Myofibrillar, 4,Endocardial Fibroelastosis,Dysphagia,Foot Drop,Centronuclear Myopathy,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Central Core Myopathy,Myopathy, Spheroid Body,Strabismus,Primary Cutaneous Amyloidosis,Distal Arthrogryposis,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Multiple Pterygium Syndrome, Lethal Type,Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome,Left Ventricular Noncompaction,Batten-Turner Congenital Myopathy,Nemaline Myopathy 2,Multiple Pterygium Syndrome, Escobar Variant

Rh Isoimmunization,Blood Group Incompatibility,Otopalatodigital Syndrome Spectrum Disorder,Congenital Autosomal Recessive Small-Platelet Thrombocytopenia,Glucosephosphate Dehydrogenase Deficiency,Thrombocytopenia 3,Hereditary Thrombocytopenia With Normal Platelets,Thrombocytopenia,Melnick-Needles Syndrome