Farber Lipogranulomatosis
A sphingolipidosis subtype that is characterized by the histological appearance of granulomatous deposits in tissues. It results from the accumulation of CERAMIDES in various tissues due to an inherited deficiency of ACID CERAMIDASE.
推出的年份: 2009
树号: C10.228.140.163.100.435.825.250, C16.320.565.189.435.825.250, C16.320.565.398.641.803.325, C16.320.565.595.554.825.250, C18.452.132.100.435.825.250, C18.452.584.563.641.803.325, C18.452.648.189.435.825.250, C18.452.648.398.641.803.325, C18.452.648.595.554.825.250
MeSH 单一 ID: D055577
进入的组:
Lipogranulomatosis, Farber
Ceramidase Deficiency
Ceramidase Deficiencies
Deficiencies, Ceramidase
Deficiency, Ceramidase
Farber's Disease
Disease, Farber's
Diseases, Farber's
Farber's Diseases
Farbers Disease
N-Laurylsphingosine Deacylase Deficiency
Deficiencies, N-Laurylsphingosine Deacylase
Deficiency, N-Laurylsphingosine Deacylase
N Laurylsphingosine Deacylase Deficiency
N-Laurylsphingosine Deacylase Deficiencies
Acid Ceramidase Deficiency
Acid Ceramidase Deficiencies
Ceramidase Deficiency, Acid
Deficiency, Acid Ceramidase
Farber Disease
早前的内容:
Lipid Metabolism (1952-1976)
Lipid Metabolism, Inborn Errors (1987-2008)
Lipidoses (1976-2008)
Sphingolipidoses (1992-2008)
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