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Descriptor English: Hyperoxaluria, Primary
Descriptor Spanish: Hiperoxaluria Primaria
Descriptor hiperoxaluria primaria
Entry term(s) oxalosis primaria
oxaluria primaria
Scope note: Cualquiera de los dos trastornos genéticos que se caracterizan por excreción urinaria de grandes cantidades de oxalato, con nefrolitiasis, nefrocalcinosis, comienzo precoz de insuficiencia renal y, con freecuencia, depósito generalizado de oxalato de calcio, resultante de un defecto en el metabolismo del glioxalato.
Descriptor Portuguese: Hiperoxalúria Primária
Descriptor French: Hyperoxalurie primaire
Entry term(s): Hyperoxalurias, Primary
Oxaloses, Primary
Oxalosis, Primary
Oxaluria, Primary
Oxalurias, Primary
Primary Hyperoxaluria
Primary Hyperoxalurias
Primary Oxaloses
Primary Oxalosis
Primary Oxaluria
Primary Oxalurias
Tree number(s): C12.050.351.968.419.313.500
C12.200.777.419.313.500
C12.950.419.313.500
C16.320.565.202.460
C18.452.648.202.460
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D006960
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 91; was see under HYPEROXALURIA 1987-90
History Note: 91(87); was see under HYPEROXALURIA 1987-90
DeCS ID: 19195
Unique ID: D006960
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1986/04/18
Revision Date: 2013/07/08
Hyperoxaluria, Primary - Preferred
Concept UI M0010843
Scope note 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.
Preferred term Hyperoxaluria, Primary
Entry term(s) Hyperoxalurias, Primary
Oxaluria, Primary
Oxalurias, Primary
Primary Hyperoxaluria
Primary Hyperoxalurias
Primary Oxaluria
Primary Oxalurias
Primary Oxalosis - Related but not broader or narrower
Concept UI M0584934
Preferred term Primary Oxalosis
Entry term(s) Oxaloses, Primary
Oxalosis, Primary
Primary Oxaloses



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