A benign, usually encapsulated slow growing tumor composed of Schwann cells. It affects peripheral and cranial nerves. It recurs infrequently and only rare cases associated with malignant transformation have been reported. [ NCIT:C3269 ]
Synonyms: schwannoma, benign benign neurilemmoma neurinoma psammomatous schwannoma peripheral fibroblastoma neurilemmoma schwannoma (WHO grade I) schwannoma benign schwannoma
Term information
- DOID:3192 (MONDO:equivalentTo)
- MedDRA:10029234 (Orphanet:252164/e)
- Orphanet:252164 (MONDO:equivalentTo)
- EFO:0000693 (MONDO:equivalentTo)
- DOID:955 (MONDO:equivalentTo)
- MEDGEN:45053 (MONDO:equivalentTo)
- GARD:4767 (MONDO:GARD)
- ICD9:215.9 (MONDO:relatedTo)
- MedDRA:10029235 (Orphanet:252164/e)
- ONCOTREE:SCHW (MONDO:equivalentTo)
- SCTID:404022001 (MONDO:equivalentTo)
- ICDO:9560/0 (NCIT:C3269)
- UMLS:C0027809 (MONDO:equivalentTo)
- NCIT:C3269 (MONDO:equivalentTo)
- NANDO:2200103 (https://orcid.org/0000-0003-0011-764X)
ordo_disorder, gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_included, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, orphanet_rare, harrisons_view_nervous_system_disorder
http://purl.obolibrary.org/obo/DOID_955
http://www.orpha.net/ORDO/Orphanet_252164
http://purl.obolibrary.org/obo/NCIT_C3269
http://linkedlifedata.com/resource/umls/id/C0027809
http://purl.obolibrary.org/obo/DOID_3192
http://www.ebi.ac.uk/efo/EFO_0000693
http://identifiers.org/medgen/45053
http://identifiers.org/snomedct/404022001