The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Muscular Dystrophies, Limb-Girdle
Hierarchy: | ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle 8 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle ∟ ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle ∟ ∟ ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle ∟ ∟ ∟ ∟ ∟ Muscular Dystrophies, Limb-Girdle |
History note: | Muscular Dystrophies (1966-2004)X |
historyNote*: | 2005; use MUSCULAR DYSTROPHIES 2000-2004
X |
publicMeSHNote*: | 2005; see MUSCULAR DYSTROPHIES 2000-2004
X |
Scope note: | A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
X |
activeMeSHYear*: | |
dateCreated*: | 2004-07-07X |
dateEstablished*: | 2005-01-01X |
dateRevised*: | 2005-06-30X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | agsX |
recordOriginator*: | lktX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Hartia-lantiodystrofiat (fi) XHartia-lantiolihasdystrofia (fi, replaced) Lihasdystrofia, hartia-lantio- (fi, replaced) Hartia-lantiolihasdystrofi (fi, replaced) Hartia-lantiodystrofia (fi, replaced) Limb-Girdle Muscular Dystrophy (en, replaced) Muscular Dystrophy, Limb-Girdle (en, replaced) Limb-Girdle Muscular Dystrophies (en, replaced) Dystrophia musculorum gingulorum membrorum (la-FI, replaced) |
Share: |
Loading results...