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bn:03829910n
Noun Concept
Categories: Autosomal dominant disorders, Myoneural junction and neuromuscular diseases, Rare diseases, Diseases named for discoverer, Collagen disease
EN
Bethlem myopathy  Benign autosomal dominant myopathy  benign congenital muscular dystrophy  Beth Rem myopathy  BETHLEM MYOPATHY 1; BTHLM1
EN
Bethlem myopathy is predominantly an autosomal dominant myopathy, classified as a congenital form of muscular dystrophy. Wikipedia
Definitions
Relations
Sources
EN
Bethlem myopathy is predominantly an autosomal dominant myopathy, classified as a congenital form of muscular dystrophy. Wikipedia
Human disease Wikidata
IS A
disease
congenital muscular dystrophy
GENETIC ASSOCIATION
COL6A1
COL6A2
COL6A3
Wikipedia
EN
Bethlem myopathy
Wikidata
EN
Bethlem myopathy
Wikipedia Redirections
EN
Benign autosomal dominant myopathy
Wikidata Alias
EN
benign congenital muscular dystrophy, Beth Rem myopathy, Bethlem Myopathy, BETHLEM MYOPATHY 1; BTHLM1, BTHLM1, Muscular Dystrophy, Benign Congenital, Myopathy, Benign Congenital, With Contractures

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