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. [ https://orcid.org/0000-0002-6601-2165 http://en.wikipedia.org/wiki/Neurofibromatosis NCIT:C6727 ]
Synonyms: type IV neurofibromatosis of riccardi acoustic neurofibromatosis von Reklinghausen disease neurofibromatosis Recklinghausen's neurofibromatosis peripheral Neurofibromatosis central Neurofibromatosis neurofibromatosis syndrome
Term information
- ICD9:237.70 (MONDO:i2s)
- NANDO:1200226 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:58149 (MONDO:equivalentTo)
- ICDO:9540/1 (NCIT:C6727)
- EFO:0008514 (MONDO:equivalentTo)
- ICD9:237.72 (DOID:8712)
- ICD9:237.71 (DOID:8712)
- UMLS:C0162678 (MONDO:equivalentTo)
- DOID:8712 (MONDO:equivalentTo)
- MESH:D017253 (MONDO:equivalentTo)
- NANDO:2201003 (https://orcid.org/0000-0003-0011-764X)
- ICD9:237.7 (DOID:8712)
- NANDO:1200225 (https://orcid.org/0000-0003-0011-764X)
- GARD:10420 (MONDO:GARD)
- SCTID:19133005 (MONDO:equivalentTo)
- NCIT:C6727 (MONDO:equivalentTo)
- NANDO:1200227 (https://orcid.org/0000-0003-0011-764X)
gard_rare, otar, rare, nord_rare
http://linkedlifedata.com/resource/umls/id/C0162678
http://identifiers.org/medgen/58149
http://purl.obolibrary.org/obo/DOID_8712
http://identifiers.org/mesh/D017253
http://purl.obolibrary.org/obo/NCIT_C6727
http://identifiers.org/snomedct/19133005