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bn:00027746n
Noun Concept
Categories: Muscular dystrophy
EN
distal muscular dystrophy  distal myopathy  Distal muscular dystrophies  distal myopathies  Distal myopathy type 3
EN
A form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant WordNet 3.0
Definitions
Relations
Sources
EN
A form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant WordNet 3.0 & Open English WordNet
Distal myopathy is a group of rare genetic disorders that cause muscle damage and weakness, predominantly in the hands and/or feet. Wikipedia
Group of genetic disorders characterized by progressive muscular atrophy and muscle weakness beginning in the hands, the legs, or the feet Wikidata
IS A
muscular dystrophy
disease
HAS KIND
Laing early-onset distal myopathy
tibial muscular dystrophy
distal muscular dystrophy 4
HEALTH SPECIALTY
neurology
WordNet 3.0 & Open English WordNet
EN
distal muscular dystrophy
Wikipedia
EN
distal myopathy
Wikidata
EN
distal muscular dystrophy
Wikipedia Redirections
EN
Distal muscular dystrophies, distal muscular dystrophy, Distal myopathies, Hedesunda disease, Miyoshi myopathy, Welander's disease, Welander distal myopathy
Wikidata Alias
EN
Distal muscular dystrophy, distal myopathies, Distal myopathy, distal myopathy, Distal myopathy type 3, Miyoshi muscular dystrophy, MPD3, MYOPATHY, DISTAL, 3, MYOPATHY, DISTAL, 3; MPD3

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