renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions
A group of kidney carcinomas characterized by the presence of different translocations involving the chromosome Xp11.2. These translocations result in the creation of gene fusions involving the TFE3 gene. Patients are usually children and young adults. Morphologically, the malignant epithelial cells form papillary patterns. [ NCIT:C27891 ]
Term info
- ONCOTREE:TRCC (MONDO:equivalentTo)
- EFO:1000508 (MONDO:equivalentTo)
- ICDO:0000/0 (NCIT:C27891)
- NCIT:C27891 (MONDO:exact-label-match)
- UMLS:C1337036 (NCIT:C27891)
A group of kidney carcinomas characterized by the presence of different translocations involving the chromosome Xp11.2. These translocations result in the creation of gene fusions involving the TFE3 gene. Patients are usually children and young adults. Morphologically, the malignant epithelial cells form papillary patterns.
http://purl.obolibrary.org/obo/NCIT_C27891, http://linkedlifedata.com/resource/umls/id/C1337036
Xp11.2 translocation-related renal cell carcinoma, renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions, tRCC, TFE3-Rearranged renal cell carcinoma, renal cell cancer associated with Xp11.2 translocations/TFE3 Gene fusions
translocation-associated renal cell carcinoma
MONDO:0006397