A tumor-prone disorder characterized by the development of multiple schwannomas and meningiomas. [ Orphanet:637 ]
Synonyms: bilateral acoustic neurofibromatosis neurofibromatosis type 2 central neurofibromatosis NF2 neurofibromatosis 2
Term information
- GARD:7193 (Orphanet:637)
- MedDRA:10029271 (Orphanet:637/e)
- DOID:0111252 (MONDO:equivalentTo)
- MESH:D009464 (Orphanet:637/e)
- SCTID:92503002 (MONDO:equivalentTo)
- NCIT:C3274 (MONDO:equivalentTo)
- Orphanet:637 (OMIM:101000)
- ICD10CM:Q85.02 (MONDO:equivalentTo)
- OMIM:101000 (Orphanet:637/e)
- UMLS:C0027832 (Orphanet:637/e)
- MedDRA:10000523 (Orphanet:637/e)
- ICD9:237.72 (MONDO:i2s)
gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen
http://purl.obolibrary.org/obo/NCIT_C3274
http://linkedlifedata.com/resource/umls/id/C0027832
http://purl.bioontology.org/ontology/ICD10CM/Q85.02
http://purl.obolibrary.org/obo/DOID_0111252
http://www.orpha.net/ORDO/Orphanet_637
http://identifiers.org/snomedct/92503002
https://omim.org/entry/101000
acoustic Schwannomas, bilateral
neurofibromatosis type II
neurofibromatosis central type
neurofibromatosis, central type
neurofibromatosis, type II
acoustic neurinoma bilateral
acoustic schwannomas bilateral
acoustic neurinoma, bilateral
neurofibromatosis, type 2