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leiomyosarcoma

Go to external page http://purl.obolibrary.org/obo/MONDO_0005058

An uncommon, aggressive malignant smooth muscle neoplasm, usually occurring in post-menopausal women. It is characterized by a proliferation of neoplastic spindle cells. Morphologic variants include epithelioid, granular cell, inflammatory and myxoid leimyosarcomas. [ NCIT:C3158 ]

Synonyms: leiomyosarcoma leiomyosarcoma, malignant leiomyosarcoma (excluding uterine leiomyosarcoma) leiomyosarcoma - not uterine Leiomyosarcomas

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C3158 (MONDO:equivalentTo)
  • MESH:D007890 (Orphanet:64720/e)
  • MedDRA:10024189 (Orphanet:64720/e)
  • DOID:1967 (MONDO:equivalentTo)
  • NORD:1356 (MONDO:NORD)
  • ONCOTREE:LMS (MONDO:equivalentTo)
  • GARD:6880 (MONDO:GARD)
  • EFO:0000564 (MONDO:equivalentTo)
  • ICD9:171.9 (MONDO:relatedTo)
  • MEDGEN:9711 (MONDO:equivalentTo)
  • Orphanet:64720 (MONDO:equivalentTo)
  • UMLS:C0023269 (MONDO:equivalentTo)
  • ICDO:8890/3 (NCIT:C3158)
  • SCTID:443719001 (MONDO:equivalentTo)
  • NANDO:2200064 (https://orcid.org/0000-0003-0011-764X)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

closeMatch

http://identifiers.org/meddra/10024189

exactMatch

http://www.orpha.net/ORDO/Orphanet_64720

http://purl.obolibrary.org/obo/NCIT_C3158

http://identifiers.org/mesh/D007890

http://identifiers.org/medgen/9711

http://linkedlifedata.com/resource/umls/id/C0023269

http://purl.obolibrary.org/obo/DOID_1967

http://identifiers.org/snomedct/443719001

excluded from qc check

http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql

id

MONDO:0005058

seeAlso

https://rarediseases.info.nih.gov/diseases/6880/leiomyosarcoma