Search on: FARBER LIPOGRANULOMATOSIS 
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Descriptor English:   Farber Lipogranulomatosis 
Descriptor Spanish:   Lipogranulomatosis de Farber 
Descriptor Portuguese:   Lipogranulomatose de Farber 
Synonyms English:   Acid Ceramidase Deficiency
Ceramidase Deficiency
Farber Disease
Farber's Disease
N-Laurylsphingosine Deacylase Deficiency
Acid Ceramidase Deficiencies
Ceramidase Deficiencies
Ceramidase Deficiency, Acid
Deficiencies, Ceramidase
Deficiencies, N-Laurylsphingosine Deacylase
Deficiency, Acid Ceramidase
Deficiency, Ceramidase
Deficiency, N-Laurylsphingosine Deacylase
Disease, Farber's
Diseases, Farber's
Farber's Diseases
Farbers Disease
Lipogranulomatosis, Farber
N Laurylsphingosine Deacylase Deficiency
N-Laurylsphingosine Deacylase Deficiencies  
Tree Number:   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
C18.452.584.687.803.325
C18.452.648.189.435.825.250
C18.452.648.398.641.803.325
C18.452.648.595.554.825.250
Definition English:   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. 
History Note English:   2009 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   53092 
Unique Identifier:   D055577 

Occurrence in VHL:
 
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