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rhabdomyosarcoma

Go to external page http://purl.obolibrary.org/obo/MONDO_0005212

A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites. [ NCIT:C3359 ]

Synonyms: rhabdomyosarcoma, malignant rhabdomyosarcoma (disease) rhabdomyosarcoma

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0035412 (MONDO:equivalentTo)
  • SCTID:302847003 (MONDO:equivalentTo)
  • MEDGEN:20561 (MONDO:equivalentTo)
  • DOID:3247 (MONDO:equivalentTo)
  • GARD:11951 (MONDO:GARD)
  • Orphanet:780 (MONDO:equivalentTo)
  • MESH:D012208 (Orphanet:780/e)
  • EFO:0002918 (MONDO:equivalentTo)
  • ONCOTREE:RMS (MONDO:equivalentTo)
  • NANDO:2200056 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C3359 (MONDO:equivalentTo)
  • MedDRA:10039022 (Orphanet:780/e)
  • ICD9:171.9 (MONDO:relatedTo)
  • HP:0002859 (MONDO:otherHierarchy)
  • ICDO:8900/3 (NCIT:C3359)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

IAO 0000589

rhabdomyosarcoma (disease)

closeMatch

http://identifiers.org/meddra/10039022

exactMatch

http://identifiers.org/snomedct/302847003

http://purl.obolibrary.org/obo/DOID_3247

http://identifiers.org/medgen/20561

http://purl.obolibrary.org/obo/NCIT_C3359

http://www.orpha.net/ORDO/Orphanet_780

http://linkedlifedata.com/resource/umls/id/C0035412

http://identifiers.org/mesh/D012208

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0016123

http://purl.obolibrary.org/obo/MONDO_0002847

id

MONDO:0005212

Term relations

Subclass of: