Search on: OXALURIA, PRIMARY 
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Descriptor English:   Hyperoxaluria, Primary 
Descriptor Spanish:   Hiperoxaluria Primaria 
Descriptor Portuguese:   Hiperoxalúria Primária 
Synonyms English:   Oxaluria, Primary  
Tree Number:   C12.777.419.313.500
C13.351.968.419.313.500
C16.320.565.202.460
C18.452.648.202.460
Definition English:   A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism. 
History Note English:   91(87); was see under HYPEROXALURIA 1987-90 
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:   19195 
Unique Identifier:   D006960 

Occurrence in VHL:
 

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