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neurofibromatosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0021061

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. [ MONDO:cjm NCIT:C6727 http://en.wikipedia.org/wiki/Neurofibromatosis ]

Synonyms: type IV neurofibromatosis of riccardi acoustic neurofibromatosis von Reklinghausen disease neurofibromatosis Recklinghausen's neurofibromatosis peripheral Neurofibromatosis central Neurofibromatosis neurofibromatosis syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:237.70 (MONDO:i2s)
  • ICD9:237.7 (DOID:8712)
  • MESH:D017253 (MONDO:equivalentTo)
  • UMLS:C0162678 (NCIT:C6727)
  • ICD9:237.72 (DOID:8712)
  • SCTID:19133005 (MONDO:equivalentTo)
  • ICD9:237.71 (DOID:8712)
  • NCIT:C6727 (MONDO:equivalentTo)
  • ICDO:9540/1 (NCIT:C6727)
  • DOID:8712 (MONDO:equivalentTo)
Subsets

rare, nord_rare

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 narrow synonym

neurofibromatosis type IV

neurofibromatosis type 4

neurofibromatosis type 2

id

MONDO:0021061