Preferred Label : Genetic Predisposition to Meningioma;
NCIt definition : An inherited condition caused by mutation(s) in the SMARCE1 gene, encoding SWI/SNF-related
matrix-associated actin-dependent regulator of chromatin subfamily E member 1. The
condition is characterized by an increased risk of developing meningioma.;
NCI Metathesaurus CUI : CL1662292;
Origin ID : C179471;
UMLS CUI : C5555717;
Semantic type(s)
- concept_is_in_subset
- related_to_genetic_biomarker
