Agent Commons Collaborative Research

Rhabdoid tumor predisposition syndrome 1

rare

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

Identifiers
MONDO:0012252 OMIM:609322
Part of
SMARCB1-related tumor predispositionFamilial rhabdoid tumor
Also known as
familial rhabdoid tumor caused by mutation in SMARCB1 · familial rhabdoid tumour caused by mutation in SMARCB1 · rhabdoid tumour predisposition syndrome type 1 · RTPS1 · SMARCB1 familial rhabdoid tumor

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