KEGG   DISEASE: Becker muscular dystrophy
Entry
H01964                      Disease                                
Name
Becker muscular dystrophy
  Supergrp
Dystrophinopathies [DS:H00562]
Description
Becker muscular dystrophy (BMD) is an X-linked neuromuscular disorder principally affecting males. It is caused by mutations in the DMD gene, which codes for dystrophin. In Becker muscular dystrophy, the distribution of muscle wasting and weakness is closely similar to that in Duchenne muscular dystrophy [DS:H01963], but the course of the disease is more benign.
Category
Nervous system disease; Musculoskeletal disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 08 Diseases of the nervous system
  Diseases of neuromuscular junction or muscle
   Primary disorders of muscles
    8C70  Muscular dystrophy
     H01964  Becker muscular dystrophy
Gene
DMD [HSA:1756] [KO:K10366]
Other DBs
ICD-11: 8C70.0
ICD-10: G71.0
MeSH: D020388
OMIM: 300376
Reference
PMID:2063877
  Authors
Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM
  Title
Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.
  Journal
Am J Hum Genet 49:54-67 (1991)
Reference
  Authors
Emery AE
  Title
The muscular dystrophies.
  Journal
Lancet 359:687-95 (2002)
DOI:10.1016/S0140-6736(02)07815-7
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