- autosomal recessive limb-girdle muscular dystrophy
- 常染色体隐性肢带肌营养不良
Medical Chinese dictionary (湘雅医学词典). 2013.
autosomal recessive limb-girdle muscular dystrophy
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Limb-girdle muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 … Wikipedia
limb-girdle muscular dystrophy — noun an autosomal recessive form of muscular dystrophy that appears anywhere from late childhood to middle age; characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle; usually progresses slowly with… … Useful english dictionary
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
autosomal recessive defect — noun a disease caused by the presence of two recessive mutant genes on an autosome • Syn: ↑autosomal recessive disease • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital … Useful english dictionary
autosomal recessive disease — noun a disease caused by the presence of two recessive mutant genes on an autosome • Syn: ↑autosomal recessive defect • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital di … Useful english dictionary
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
Congenital muscular dystrophy — Classification and external resources ICD 10 G71.2 ICD 9 359.0 … 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
Dysferlin — Dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) Identifiers Symbols DYSF; FER1L1; FLJ00175; FLJ90168; LGMD2B External IDs … Wikipedia
SGCD — Sarcoglycan, delta (35kDa dystrophin associated glycoprotein), also known as SGCD, is a human gene.cite web | title = Entrez Gene: SGCD sarcoglycan, delta (35kDa dystrophin associated glycoprotein)| url =… … Wikipedia
