Expresión de búsqueda: FARBER LIPOGRANULOMATOSIS 
Descriptores Encontrados: 1
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Descriptor Inglés:   Farber Lipogranulomatosis 
Descriptor Español:   lipogranulomatosis de Farber 
Descriptor Portugués:   Lipogranulomatose de Farber 
Sinónimos Inglés:   Acid Ceramidase Deficiencies
Acid Ceramidase Deficiency
Ceramidase Deficiencies
Ceramidase Deficiency
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 Disease
Farber's Disease
Farber's Diseases
Farbers Disease
Lipogranulomatosis, Farber
N Laurylsphingosine Deacylase Deficiency
N-Laurylsphingosine Deacylase Deficiencies
N-Laurylsphingosine Deacylase Deficiency  
Categoría:   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
Definición Inglés:   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. 
Nota Histórica Inglés:   2009 
Calificadores Permitidos Inglés:  
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
Número del Registro:   53092 
Identificador Único:   D055577 

Ocurrencia en la BVS: 		 

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