Search on: NIEMANN-PICK DISEASE, TYPE A 
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Descriptor English:   Niemann-Pick Disease, Type A 
Descriptor Spanish:   Enfermedad de Niemann-Pick Tipo A 
Descriptor Portuguese:   Doença de Niemann-Pick Tipo A 
Synonyms English:   Sphingomyelinase Deficiency Disease  
Tree Number:   C10.228.140.163.100.435.825.700.500
C15.604.250.410.625.500
C16.320.565.189.435.825.700.500
C16.320.565.398.641.803.730.500
C16.320.565.595.554.825.700.500
C18.452.132.100.435.825.700.500
C18.452.584.687.803.730.500
C18.452.648.189.435.825.700.500
C18.452.648.398.641.803.730.500
C18.452.648.595.554.825.700.500
Definition English:   The classic infantile form of Niemann-Pick Disease, caused by mutation in SPHINGOMYELIN PHOSPHODIESTERASE. It is characterized by accumulation of SPHINGOMYELINS in the cells of the MONONUCLEAR PHAGOCYTE SYSTEM and other cell throughout the body leading to cell death. Clinical signs include JAUNDICE, hepatosplenomegaly, and severe brain damage. 
History Note English:   2007; use NIEMANN-PICK DISEASES 2000-2006 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
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
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   52105 
Unique Identifier:   D052536 

Occurrence in VHL:
 

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