Rhabdoid tumor predisposition syndrome 2

Any familial rhabdoid tumor in which the cause of the disease is a mutation in the SMARCA4 gene.

Also known as: SMARCA4 familial rhabdoid tumor, SMARCA4 familial rhabdoid tumour, familial rhabdoid tumor caused by mutation in SMARCA4, familial rhabdoid tumour caused by mutation in SMARCA4, rhabdoid tumor predisposition syndrome 2, rhabdoid tumor predisposition syndrome type 2, rhabdoid tumour predisposition syndrome type 2, RTPS2

2891 clinical trials for this condition and its sub-types, 1 tagged with Rhabdoid tumor predisposition syndrome 2 itself.