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 |