schwannomatosis SMARCB1-related schwannomatosis https://github.com/monarch-initiative/mondo/issues/10438 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/7663 https://github.com/monarch-initiative/mondo/issues/8567 https://www.malacards.org/card/schwannomatosis_1_2 MONDO:0024517 GARD:0025408 MEDGEN:887689 SMARCB1 schwannomatosis 1 A susceptibility to the development of schwannomatosis conferred by germline mutation in the SMARCB1 gene, characterized by the onset of multiple intracranial, spinal, or peripheral schwannomas, without involvement of the vestibular nerve. Affected individuals may also have multiple meningiomas. SWNTS1 DOID:0070480 NCIT:C186703 neurilemmomatosis, congenital cutaneous schwannomatosis 1 OMIM:162091 schwannomatosis-1, susceptibility to UMLS:C4048809 SMARCB1-related tumor predisposition