A hereditary neoplastic syndrome in which tumors grow in the nervous system. There are typically 3 main types recognized, but other forms with uncertain etiology exist. [ NCIT:C6727 https://en.wikipedia.org/wiki/Neurofibromatosis MONDO:cjm ]

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C6727 (MONDO:equivalentTo)
  • DOID:8712 (MONDO:equivalentTo)
  • SCTID:19133005 (MONDO:equivalentTo)
  • ICD9:237.71 (MONDO:superClassOf)
  • GARD:0010420 (shared-umls-xref)
  • MESH:D017253 (MONDO:equivalentTo)
  • ICD9:237.70 (i2s)
  • ICD9:237.7 (DOID:8712)
  • ICD10:Q85.02 (MONDO:superClassOf)
  • ICD10:Q85.00 (DOID:8712)
  • ICD10:Q85.01 (DOID:8712)
  • ICDO:9540/1 (NCIT:C6727)
  • UMLS:C0162678 (NCIT:C6727)
  • ICD9:237.72 (MONDO:superClassOf)
  • COHD:376938 (MONDO:equivalentTo)
closeMatch

http://identifiers.org/snomedct/81669005

http://linkedlifedata.com/resource/umls/id/C0220695

http://identifiers.org/snomedct/700060008

http://identifiers.org/snomedct/700061007

http://identifiers.org/snomedct/154642000

definition

A hereditary neoplastic syndrome in which tumors grow in the nervous system. There are typically 3 main types recognized, but other forms with uncertain etiology exist.

exactMatch

http://linkedlifedata.com/resource/umls/id/C0162678

http://purl.obolibrary.org/obo/DOID_8712

http://identifiers.org/mesh/D017253

http://purl.obolibrary.org/obo/NCIT_C6727

http://identifiers.org/snomedct/19133005

has exact synonym

neurofibromatosis type IV

type IV neurofibromatosis of riccardi

neurofibromatosis type 4

acoustic neurofibromatosis

Neurofibromatosis 1

Recklinghausen's neurofibromatosis

peripheral Neurofibromatosis

neurofibromatosis type 1

von Reklinghausen disease

neurofibromatosis type 2

neurofibromatosis

central Neurofibromatosis

neurofibromatosis syndrome

id

MONDO:0021061