CUI Disease Vocabulary Name in Vocabulary Code
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency DO congenital merosin-deficient muscular dystrophy 1A 0110636
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency MONDO congenital merosin-deficient muscular dystrophy 1A 0011925
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency MSH Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency C564317
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency OMIM MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A 607855
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency OMIM MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT 607855
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency OMIM MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY 607855
C1842898 Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency ORDO Laminin subunit alpha 2-related congenital muscular dystrophy 258