- autosomal dominant limb-girdle muscular dystrophy
- 常染色体显性肢带肌营养不良
Medical Chinese dictionary (湘雅医学词典). 2013.
Medical Chinese dictionary (湘雅医学词典). 2013.
Limb-girdle muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 … Wikipedia
limb-girdle muscular dystrophy — a group of disorders characterized by progressive weakness and wasting in the pelvic girdle (pelvifemoral muscular dystrophy) or shoulder girdle (scapulohumeral muscular dystrophy). It occurs in various subtypes, some of which are of autosomal… … Medical dictionary
Muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.0 … Wikipedia
Emery–Dreifuss muscular dystrophy — For other uses of EDMD , see Everybody Draw Mohammed Day. Emery–Dreifuss muscular dystrophy Classification and external resources ICD 10 G71.0 ICD 9 … Wikipedia
Oculopharyngeal muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 … Wikipedia
Facioscapulohumeral muscular dystrophy — FSHD redirects here. For other uses, see FSHD (disambiguation). Facioscapulohumeral muscular dystrophy Classification and external resources ICD 10 G71.0 ICD 9 … Wikipedia
dystrophy — Progressive changes that may result from defective nutrition of a tissue or organ. SYN: dystrophia. [dys + G. trophe, nourishment] adiposogenital d. a disorder characterized primarily by obesity and hypogonadotrophic hypogonadism … Medical dictionary
Myotonic dystrophy — Classification and external resources ICD 10 G71.1 OMIM 160900 602668 … Wikipedia
Laminopathy — Normal nuclear lamina (a and b) and mutant nuclear lamina (c and d) from a patient with HGPS, visualized by immunofluorescence note the irregular and bumpy shape of the laminopathic nuclei[1] Laminopathies are a group of rare genetic disorders… … Wikipedia
Caveolin 3 — Caveolin 3, also known as CAV3, is a human gene.cite web | title = Entrez Gene: CAV3 caveolin 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=859| accessdate = ] PBB Summary section title = summary text … Wikipedia
Valosin-containing protein — Valosin containing protein, also known as VCP, is a human gene.cite web | title = Entrez Gene: VCP valosin containing protein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7415| accessdate = ] PBB Summary … Wikipedia