CUI Disease Vocabulary Name in Vocabulary Code
C3661489 Autosomal Dominant Myotubular Myopathy MSH Myopathy, Centronuclear D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Centronuclear Myopathy, X-Linked D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Tubular Aggregate Myopathy D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Congenital Fiber Type Disproportion D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Myopathies, Structural, Congenital D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Congenital Structural Myopathy D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Myopathy, Centronuclear, Autosomal Dominant D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Autosomal Recessive Centronuclear Myopathy D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Autosomal Dominant Myotubular Myopathy D020914
C3661489 Autosomal Dominant Myotubular Myopathy MSH Myopathy, Centronuclear, 1 D020914