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Summary Literature (0)
MIM:607174 - MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO

Xenbase Genes: nf2, mn1, pten, smarce1, pdgfb, sufu

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011789 - familial meningioma
MONDO:0016995 - familial multiple meningioma