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Descriptor English: Wilms Tumor
Descriptor Spanish: Tumor de Wilms
Descriptor tumor de Wilms
Entry term(s) nefroblastoma
tumor de Wilms bilateral
Scope note: Tumor renal maligno constituido por tres tipos de células (blastémicas, estromales y epiteliales), aunque no todas ellas están presentes en cada caso.
Descriptor Portuguese: Tumor de Wilms
Descriptor French: Tumeur de Wilms
Entry term(s): Bilateral Wilms Tumor
Nephroblastoma
Nephroblastomas
Tumor, Bilateral Wilms
Tumor, Wilms
Tumor, Wilms'
Wilm Tumor
Wilm's Tumor
Wilms Tumor 1
Wilms Tumor, Bilateral
Wilms' Tumor
Tree number(s): C04.557.435.595
C04.588.945.947.535.585
C04.700.900
C12.050.351.937.820.535.585
C12.050.351.968.419.473.585
C12.200.758.820.750.585
C12.200.777.419.473.585
C12.900.820.535.585
C12.950.419.473.585
C12.950.983.535.585
C16.320.700.900
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D009396
Scope note: A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN.
Annotation: coordinate IM with KIDNEY NEOPLASMS (IM); /genet: consider also GENES, WILMS TUMOR
Allowable Qualifiers: BL blood
BS blood supply
CF cerebrospinal fluid
CH chemistry
CI chemically induced
CL classification
CN congenital
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
SC secondary
SU surgery
TH therapy
UL ultrastructure
UR urine
VE veterinary
VI virology
Public MeSH Note: 2006; see NEPHROBLASTOMA 1994-2005, WILMS' TUMOR 1991-1993, see NEPHROBLASTOMA 1963-1990
History Note: 2006 (1963)
Related: Genes, Wilms Tumor MeSH
WT1 Proteins MeSH
DeCS ID: 31926
Unique ID: D009396
NLM Classification: WJ 358
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2006/01/01
Date of Entry: 1999/01/01
Revision Date: 2018/06/29
Wilms Tumor - Preferred
Concept UI M0014630
Scope note A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN.
Preferred term Wilms Tumor
Entry term(s) Nephroblastoma
Nephroblastomas
Tumor, Wilms
Tumor, Wilms'
Wilm Tumor
Wilm's Tumor
Wilms Tumor 1
Wilms' Tumor
Bilateral Wilms Tumor - Narrower
Concept UI M0533134
Preferred term Bilateral Wilms Tumor
Entry term(s) Tumor, Bilateral Wilms
Wilms Tumor, Bilateral



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