Agent Commons Collaborative Research
Rhabdoid tumor predisposition syndrome 2
rareAny familial rhabdoid tumor in which the cause of the disease is a mutation in the SMARCA4 gene.
- Identifiers
- MONDO:0013224 OMIM:613325
- Causal genes
- SMARCA4
- Also known as
- familial rhabdoid tumor caused by mutation in SMARCA4 · familial rhabdoid tumour caused by mutation in SMARCA4 · rhabdoid tumor predisposition syndrome type 2 · rhabdoid tumour predisposition syndrome type 2 · RTPS2
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