Concept information
Preferred term
Wilms Tumor
Type
-
mesh:Descriptor
Definition
- 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.
Narrower concepts
Entry terms
- Nephroblastoma
- Wilms' Tumor
- Wilms Tumor 1
Allowable Qualifier(s)
- blood (Qualifier)
- blood supply (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- chemistry (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- congenital (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- secondary (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- ultrastructure (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Néphroblastome
-
Tumeur de Birch-Hirschfeld
URI
http://data.loterre.fr/ark:/67375/JVR-PBGMNZDQ-3
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