An embryonal pediatric tumor of the kidney which may also be seen rarely in adults. The peak incidence of Wilms tumor is between the second and fifth year of life. Microscopically, it is composed of a mixture of cellular elements (blastemal, stromal, and epithelial). The most common sites of metastasis include the regional lymph nodes, lungs, and liver. [ NCIT:C40407 ]
Synonyms: renal embryonic tumor nephroblastoma, malignant renal Wilms tumor kidney Wilms tumor Wilms tumor of the kidney renal Wilms' tumor renal embryonic tumour Wilms' tumour of the kidney nephroblastoma Wilms tumour of the kidney Wilms' tumor of the kidney renal Wilms' tumour renal Wilms tumour
Term information
- ONCOTREE:WT (MONDO:equivalentTo)
- ICDO:8960/3 (NCIT:C40407)
- DOID:5176 (MONDO:equivalentTo)
- Orphanet:654 (MONDO:equivalentTo)
- GARD:7892 (Orphanet:654)
- MedDRA:10029145 (Orphanet:654/e)
- SCTID:302849000 (MONDO:equivalentTo)
- NCIT:C40407 (MONDO:equivalentTo)
- DOID:2154 (MONDO:equivalentTo)
- NORD:1855 (MONDO:NORD)
gard_rare, ordo_disease, rare, nord_rare, orphanet_rare
http://www.orpha.net/ORDO/Orphanet_654
http://purl.obolibrary.org/obo/DOID_5176
http://purl.obolibrary.org/obo/NCIT_C40407
http://purl.obolibrary.org/obo/DOID_2154
http://identifiers.org/snomedct/302849000
childhood renal Wilms tumor
nonanaplastic renal Wilm's tumor
childhood renal Wilms' cancer
nonanaplastic renal Wilm's tumour
childhood renal Wilms tumour
embryonal nephroma
adult renal Wilms' tumour
adult nephroblastoma