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ENMuscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency (MDCI)
Alias:
Congenital Muscular Dystrophy Due to Integrin Alpha-7 Deficiency
Congenital Muscular Dystrophy with Integrin Alpha-7 Deficiency
Muscular Dystrophy, Congenital, Due to Itga7 Deficiency
Congenital Myopathy Due to Integrin Alpha-7 Deficiency
Congenital Muscular Dystrophy with Itga7 Deficiency
Dystrophy, Muscular, Congenital, Due to Integrin Alpha-7 Deficiency
Muscular Dystrophy Congenital Due to Integrin Alpha-7 Deficiency
Myopathy, Congenital, Due to Integrin Alpha-7 Deficiency
Mdci
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Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency, also known as congenital muscular dystrophy due to integrin alpha-7 deficiency, is related to muscular dystrophy-dystroglycanopathy , type c, 7 and brazilian hemorrhagic fever. An important gene associated with Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency is ITGA7 (Integrin Subunit Alpha 7), and among its related pathways/superpathways are Extracellular matrix organization and Non-integrin membrane-ECM interactions. Affiliated tissues include skeletal muscle and lung, and related phenotypes are muscle weakness and motor delay
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