| Disease Aliases (28) | Atrophie blanche Cmd1a Cmd1a - congenital muscular dystrophy type 1a Congenital muscular dystrophy due to laminin alpha2 deficiency Congenital muscular dystrophy type 1a Lama2 congenital muscular dystrophy Lama2-related muscular dystrophy Laminin alpha-2 deficiency Laminin subunit alpha 2-related congenital muscular dystrophy Mcd1a - muscular congenital dystrophy type 1a Mdc1a Muscular dystrophy, congenital merosin-deficient Muscular dystrophy, congenital, due to partial lama2 deficiency Merosin deficient congenital muscular dystrophy Merosin-deficient congenital muscular dystrophy type 1a Merosin-deficient congenital muscular dystrophy Merosin-negative congenital muscular dystrophy Muscular dystrophy, congenital merosin-deficient, 1a Muscular dystrophy congenital, merosin negative Muscular dystrophy white matter spongiosis Muscular dystrophy, congenital, merosin-deficient Muscular dystrophy, congenital, merosin-deficient 1a Congenital merosin-deficient muscular dystrophy 1a Congenital merosin-deficient muscular dystrophy type 1a Congenital muscular dystrophy caused by mutation in lama2 Muscular dystrophy, congenital merosin-deficient, 1a; mdc1a Muscular dystrophy, congenital merosin-deficient, type 1a Muscular dystrophy-white matter spongiosis syndrome |
Associated Genes (1) NCBI-RefSeq: LAMA2 (Laminin subunit alpha 2) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Merosin deficient congenital muscular dystrophy | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |