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764694005: carcinome rénal associé à une translocation de la famille MiT (trouble)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3654221010 Translocation renal cell carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3654704017 MiT family translocation renal cell carcinoma en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3654705016 MiT family translocation renal cell carcinoma (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
767031000241114 carcinome rénal associé à une translocation de la famille MiT (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
900271000172118 carcinome rénal associé à une translocation MITF/TFE fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
997881000172117 carcinome rénal associé à une translocation de la famille MiT fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3654711018 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3654712013 A rare subtype of renal cell carcinoma with recurrent genetic abnormalities, harbouring 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 haematuria, flank pain, palpable abdominal mass and/or systemic symptoms of anaemia, fatigue and fever. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
MiT family translocation renal cell carcinoma est un(e) (attribut) Renal cell carcinoma true Inferred relationship Some
MiT family translocation renal cell carcinoma morphologie associée (attribut) MiT family translocation renal cell carcinoma (morphologic abnormality) true Inferred relationship Some 1
MiT family translocation renal cell carcinoma localisation d'une constatation (attribut) structure d'un rein true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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