bn:03130798n
Noun Concept
Categories: Musculoskeletal disease stubs, Rare diseases, Autosomal dominant disorders, Myoneural junction and neuromuscular diseases
EN
zaspopathy  myofibrillar myopathy 4  Late-onset distal myopathy, Markesbery-Griggs type  MFM4  myofibrillar myopathy type 4
EN
Zaspopathy, also called ZASP-related myofibril myopathy, is a novel autosomal dominant form of progressive muscular dystrophy, first described in 2005. Wikipedia
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EN
Zaspopathy, also called ZASP-related myofibril myopathy, is a novel autosomal dominant form of progressive muscular dystrophy, first described in 2005. Wikipedia
Human disease Wikidata