Rhabdoid tumor predisposition syndrome 1

MONDO:0012252

Any familial rhabdoid tumor in which the cause of the disease is a mutation in the SMARCB1 gene.

Also known as: SMARCB1 familial rhabdoid tumor, SMARCB1 familial rhabdoid tumour, familial rhabdoid tumor caused by mutation in SMARCB1, familial rhabdoid tumour caused by mutation in SMARCB1, rhabdoid tumor predisposition syndrome 1, rhabdoid tumor predisposition syndrome type 1, rhabdoid tumors, somatic, rhabdoid tumour predisposition syndrome type 1

2852 clinical trials for this condition and its sub-types, 0 tagged with Rhabdoid tumor predisposition syndrome 1 itself.

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↑ Familial rhabdoid tumor (1)

Including sub-types (2852) Tagged with Rhabdoid tumor predisposition syndrome 1 (0)

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