neurofibromatosis
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. [ NCIT:C6727 Wikipedia:Neurofibromatosis MONDO:cjm ]
Term info
- SCTID:19133005 (MONDO:equivalentTo)
- UMLS:C0162678 (NCIT:C6727)
- ICD9:237.70 (MONDO:i2s)
- NCIT:C6727 (MONDO:equivalentTo)
- ICD9:237.7 (DOID:8712)
- GARD:0010420 (MONDO:shared-umls-xref)
- MESH:D017253 (MONDO:equivalentTo)
- DOID:8712 (MONDO:equivalentTo)
- ICD9:237.72 (DOID:8712)
- ICDO:9540/1 (NCIT:C6727)
- ICD9:237.71 (DOID:8712)
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.
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
type IV neurofibromatosis of riccardi, acoustic neurofibromatosis, von Reklinghausen disease, neurofibromatosis, Recklinghausen's neurofibromatosis, peripheral Neurofibromatosis, central Neurofibromatosis, neurofibromatosis syndrome
neurofibromatosis type IV, neurofibromatosis type 4, neurofibromatosis type 2
MONDO:0021061