JSON

rhabdomyosarcoma

^ 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 ]

Term info

database cross reference
  • MedDRA:10039022 (Orphanet:780/e)
  • DOID:3247 (MONDO:equivalentTo)
  • NCIT:C3359 (MONDO:equivalentTo)
  • Orphanet:780 (MONDO:equivalentTo)
  • SCTID:302847003 (MONDO:equivalentTo)
  • ICDO:8900/3 (NCIT:C3359)
  • EFO:0002918 (MONDO:equivalentTo)
  • UMLS:C0035412 (Orphanet:780/e)
  • HP:0002859 (MONDO:otherHierarchy)
  • ONCOTREE:RMS (MONDO:equivalentTo)
  • ICD9:171.9 (MONDO:relatedTo)
  • MESH:D012208 (Orphanet:780/e)
Subsets

ordo_disease

IAO 0000589

rhabdomyosarcoma (disease)

closeMatch

http://identifiers.org/meddra/10039022

definition

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.

exactMatch

http://identifiers.org/snomedct/302847003, http://purl.obolibrary.org/obo/DOID_3247, http://purl.obolibrary.org/obo/NCIT_C3359, http://purl.obolibrary.org/obo/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

has exact synonym

rhabdomyosarcoma, malignant, rhabdomyosarcoma (disease), rhabdomyosarcoma

id

MONDO:0005212