Name | Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency |
---|---|
Synonym | Myopathy, Congenital, Due To Integrin Alpha-7 Deficiency |
Categories | Genetic disease (inborn) | Musculoskeletal disease | Nervous system disease |
MeSH® ID | C567709 |
OMIM® ID | 613204 |
1. |
Diseases
←
Musculoskeletal Diseases
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
2. |
Diseases
←
Nervous System Diseases
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
3. |
Diseases
←
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |