Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Nervous System Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
Neurofibromatoses
...
Peripheral Nervous System Diseases
Peripheral Nervous System Neoplasms
Cranial Nerve Neoplasms
Neuroma, Acoustic
...
Nervous System Neoplasms
Peripheral Nervous System Neoplasms
Cranial Nerve Neoplasms
Neuroma, Acoustic
Preferred term
Neurofibromatosis 2
Type
-
Topical Descriptor
Broader concept
Entry terms
- Acoustic Neurofibromatoses, Bilateral
- Acoustic Neurofibromatosis, Bilateral
- Bilateral Acoustic Neurofibromatoses
- Bilateral Acoustic Neurofibromatosis
- Central Neurofibromatoses
- Central Neurofibromatosis
- Central NF2 Neurofibromatoses
- Central NF2 Neurofibromatosis
- Neurofibromatoses, Bilateral Acoustic
- Neurofibromatoses, Central
- Neurofibromatoses, Central NF2
- Neurofibromatoses, Type 2
- Neurofibromatoses, Type II
- Neurofibromatosis, Acoustic, Bilateral
- Neurofibromatosis, Bilateral Acoustic
- Neurofibromatosis, Central
- Neurofibromatosis, Central NF2
- Neurofibromatosis, Central, NF 2
- Neurofibromatosis, Central, NF2
- Neurofibromatosis, central type
- Neurofibromatosis II
- Neurofibromatosis IIs
- Neurofibromatosis Type 2
- Neurofibromatosis, Type 2
- Neurofibromatosis Type II
- Neurofibromatosis, Type II
- NF2 (Neurofibromatosis 2)
- NF2s (Neurofibromatosis 2)
- Type 2 Neurofibromatoses
- Type 2 Neurofibromatosis
- Type II Neurofibromatoses
- Type II Neurofibromatosis
Note
- do not confuse with NEUROFIBROMATOSIS 1; coord IM with precoord/neopl term (IM) if relevant
Scope note
- An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.
History note
- 1992; NEUROFIBROMATOSIS, CENTRAL, NF2 use NEUROFIBROMATOSIS, CENTRAL, NF-2 use NEUROMA, ACOUSTIC 1989-1991; NEUROMA, ACOUSTIC, BILATERAL use NEUROMA, ACOUSTIC 1989-91
In other languages
-
Finnish
-
neurofibromatoosi tyyppi 2
-
neurofibromatosis 2
-
NF-II
-
NF2
-
tyypin 2 neurofibromatoosi
-
Swedish
URI
http://www.yso.fi/onto/mesh/D016518
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}