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MIT family translocation renal cell carcinoma
Disease Summary
Associated Targets (7)
Tbio
7
Mondo Description MiT family translocation renal cell carcinoma (t-RCC) is a rare subtype of renal cell carcinoma with recurrent genetic abnormalities, harboring rearrangements of the TFE3 (Xp11 t-RCC) or TFEB [t(6;11) t-RCC] genes. The t(6;11) t-RCC has distinctive histologic features of biphasic appearance with larger epitheloid and smaller eosinophilic cells. The symptoms are usually non-specific and include hematuria, flank pain, palpable abdominal mass and/or systemic symptoms of anemia, fatigue and fever.
Mondo Term and Equivalent IDs
MONDO:0017886: MIT family translocation renal cell carcinoma
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:319308
SCTID:764694005
UMLS:C4518356
MONDO:0017886
High level summary of knowledge for a disease, including descriptions and datasource references. Click the "?" for more details.