MeSH 搜索器

Mevalonate Kinase Deficiency

Autosomal recessive disorder caused by mutations in the mevalonate kinase gene. Because of the mutations cholesterol biosynthesis is disrupted and MEVALONIC ACID accumulates. It is characterized by a range of symptoms, including dysmorphic FACIES, psychomotor retardation, CATARACT, hepatosplenomegaly, CEREBELLAR ATAXIA, elevated IMMUNOGLOBULIN D, and recurrent febrile crises with FEVER; LYMPHADENOPATHY; ARTHRALGIA; EDEMA; and rash.
推出的年份: 2008
副标题
树号: C10.228.140.163.100.593, C15.378.147.542.319, C16.320.382.750, C16.320.565.189.593, C16.320.565.663.430, C18.452.132.100.593, C18.452.648.189.593, C18.452.648.663.430, C20.683.460.319
MeSH 单一 ID: D054078
进入的组:
  • Kinase Deficiencies, Mevalonate
  • Kinase Deficiency, Mevalonate
  • Mevalonate Kinase Deficiencies
  • Mevalonic Aciduria
  • Aciduria, Mevalonic
  • Mevalonicaciduria
  • Mevalonicacidurias
  • Hyperimmunoglobulinemia D
  • Hyper IgD Syndrome
  • Hyper IgD Syndromes
  • Periodic Fever, Dutch Type
  • Hyper-IgD Syndrome
  • Hyper-IgD Syndromes
  • Syndrome, Hyper-IgD
  • Hyperimmunoglobulinemia D And Periodic Fever Syndrome

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