NCI CTEP Simplified Disease Classification Terminology
NCI CTEP SDC Neurofibromatosis Sub-Category Terminology
CTRP Terminology
CTRP Disease Terminology
CPTAC Terminology
CPTAC Neoplasms Codelist
GDC Terminology
CPTAC Codelists Terminology
Mapped ICDO3.1 Terminology
Mapped ICDO3.1 Morphology Terminology
Mapped ICDO3.1 Morphology PT Terminology
NF1 Gene
NF2 Gene
Histology ICD-O Morphology Code
GDC Value Terminology
ICD-O-3 Morphology Term Diagnosis Question
Neurofibromatosis
9540/1
9540/1
An autosomal dominant hereditary neoplastic syndrome. Two distinct clinicopathological entities are recognized: neurofibromatosis type 1 and neurofibromatosis type 2. Neurofibromatosis type 1 is associated with the presence of cafe-au-lait cutaneous lesions, multiple neurofibromas, malignant peripheral nerve sheath tumors, optic nerve gliomas, and bone lesions. Neurofibromatosis type 2 is associated with the presence of schwannomas, meningiomas, and gliomas.
C0162678
C6727
CPTAC
CTEP
CTRP
Disease or Syndrome
GDC
Multiple neurofibromatosis
NICHD
Neurofibromatosis
Neurofibromatosis
Neurofibromatosis
Neurofibromatosis
Neurofibromatosis (nonmalignant)
Neurofibromatosis Syndrome
Neurofibromatosis, NOS
Neurofibromatosis, NOS
Phakomatosis
NICHD Terminology
Neonatal Research Network Terminology