CUI Disease Vocabulary Name in Vocabulary Code
C1263858 Muscular dystrophy congenital, merosin negative DO congenital merosin-deficient muscular dystrophy 1A 0110636
C1263858 Muscular dystrophy congenital, merosin negative MONDO congenital merosin-deficient muscular dystrophy 1A 0011925
C1263858 Muscular dystrophy congenital, merosin negative MSH Muscular dystrophy congenital, merosin negative C537384
C1263858 Muscular dystrophy congenital, merosin negative NCI MDC1A C118783
C1263858 Muscular dystrophy congenital, merosin negative NCI Merosin-Deficient Congenital Muscular Dystrophy Type 1A C118783
C1263858 Muscular dystrophy congenital, merosin negative OMIM MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A 607855
C1263858 Muscular dystrophy congenital, merosin negative OMIM MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT 607855
C1263858 Muscular dystrophy congenital, merosin negative OMIM MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY 607855
C1263858 Muscular dystrophy congenital, merosin negative ORDO Laminin subunit alpha 2-related congenital muscular dystrophy 258