Term info
- NCIT:C3269 (MONDO:equivalentTo)
- ICDO:9560/0 (NCIT:C3269)
- UMLS:C0027809 (Orphanet:252164/e)
- SCTID:404022001 (MONDO:equivalentTo)
- DOID:955 (MONDO:equivalentTo)
- ICD9:215.9 (MONDO:relatedTo)
- ONCOTREE:SCHW (MONDO:equivalentTo)
- MedDRA:10029235 (Orphanet:252164/e)
- MedDRA:10029234 (Orphanet:252164/e)
- DOID:3192 (MONDO:equivalentTo)
- EFO:0000693 (MONDO:equivalentTo)
- UMLS:CN202001 (MONDO:equivalentTo)
- GARD:0004767 (MONDO:equivalentTo)
- Orphanet:252164 (MONDO:equivalentTo)
gard_rare, ordo_disease
http://identifiers.org/meddra/10029235, http://identifiers.org/meddra/10029234
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.
http://purl.obolibrary.org/obo/DOID_955, http://purl.obolibrary.org/obo/Orphanet_252164, http://purl.obolibrary.org/obo/NCIT_C3269, http://linkedlifedata.com/resource/umls/id/C0027809, http://purl.obolibrary.org/obo/DOID_3192, http://linkedlifedata.com/resource/umls/id/CN202001, http://identifiers.org/snomedct/404022001
schwannoma, benign, benign neurilemmoma, neurinoma, psammomatous schwannoma, peripheral fibroblastoma, neurilemmoma, schwannoma (WHO grade I), schwannoma, benign schwannoma
neurolemmoma, SCHW
MONDO:0002546
https://rarediseases.info.nih.gov/diseases/4767/schwannoma