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Disease Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency

Name Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Categories Genetic disease (inborn) | Musculoskeletal disease | Nervous system disease
MeSH® ID C564317

Top ↑ Ancestors

1. DiseasesMusculoskeletal Diseases Has associated chemicals Has associated genes Has associated exposure references Muscular Diseases Has associated chemicals Has associated genes Muscular Disorders, Atrophic Has associated chemicals Has associated genes Muscular Dystrophies Has associated chemicals Has associated genes Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neuromuscular Diseases Has associated chemicals Has associated genes Has associated exposure references Muscular Diseases Has associated chemicals Has associated genes Muscular Disorders, Atrophic Has associated chemicals Has associated genes Muscular Dystrophies Has associated chemicals Has associated genes Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Muscular Dystrophies Has associated chemicals Has associated genes Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency

Top ↑ Descendants

None.