MeSH 搜索器

Laminopathies

Congenital neuromuscular and muscular dystrophy diseases associated with mutations in the LAMIN TYPE A (Lamin A/C or LMNA gene). It includes CARDIOMYOPATHY, DILATED, 1A; CHARCOT-MARIE-TOOTH DISEASE, type 2B1; EMERY-DREIFUSS MUSCULAR DYSTROPHY, types 2 and 3; HUTCHINSON-GILFORD PROGERIA SYNDROME; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; Malouf syndrome; Mandibuloacral dysplasia; LMNA-related muscular dystrophy; Restrictive dermopathy, lethal; Heart-hand syndrome, Slovenian type.
推出的年份: 2021
副标题
树号: C16.320.488
MeSH 单一 ID: D000083083
进入的组:
  • Laminopathy
  • LMNA-Associated Diseases
  • Disease, LMNA-Associated
  • LMNA Associated Diseases
  • LMNA-Associated Disease
  • LMNA-Linked Diseases
  • Disease, LMNA-Linked
  • LMNA Linked Diseases
  • LMNA-Linked Disease
早前的内容:
  • Cardiomyopathies (2002-2020)
  • Lamin Type A/genetics (2002-2020)
  • Neuromuscular Diseases (2002-2020)

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