MeSH 搜索器

Neuroacanthocytosis

An inherited autosomal disorder that is characterized by neurodegeneration; orofacial and buccal DYSKINESIAS; CHOREA; and thorny-looking red cells (ACANTHOCYTES). This disorder is due to mutations of chorein which is important in protein trafficking and is encoded by Vps13a on chromosome 9q21.
推出的年份: 2008(2000)
副标题
树号: C10.228.662.262.249.937, C16.320.400.550
MeSH 单一 ID: D054546
进入的组:
  • Chorea Acanthocytosis Syndrome
  • Chorea Acanthocytosis Syndromes
  • Acanthocytosis with Neurologic Disorder
  • Choreoacanthocytosis
  • Choreoacanthocytoses
  • Levine-Critchley Syndrome
  • Levine Critchley Syndrome
  • Chorea Acanthocytosis
  • Acanthocytoses, Chorea
  • Acanthocytosis, Chorea
  • Chorea Acanthocytoses
  • Chorea-Acanthocytosis
  • Chorea-Acanthocytoses
早前的内容:
  • Acanthocytes (1981-2007)
  • Hematologic Diseases (1982-2007)
  • Movement Disorders (1982-2007)

留言 (0)

沒有登入
gif