Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
...
Peripheral Nervous System Diseases
Peripheral Nervous System Neoplasms
Nerve Sheath Neoplasms
Neurofibroma
...
Nervous System Neoplasms
Peripheral Nervous System Neoplasms
Nerve Sheath Neoplasms
Neurofibroma
Preferred term
Neurofibromatoses
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Multiple Neurofibroma
- Multiple Neurofibromas
- Neurofibroma, Multiple
- Neurofibromas, Multiple
- Neurofibromatosis
- Neurofibromatosis Syndrome
- Neurofibromatosis Syndromes
- Syndrome, Neurofibromatosis
- Syndromes, Neurofibromatosis
Note
- multiple neurofibromas; specifics are available
Scope note
- A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
History note
- 2000(1993)
In other languages
-
Finnish
-
morbus von Recklinghausen
-
neurofibromatoosi
-
neurofibromatosis
-
neurofibromatosis non maligna
-
von Recklinghausen
-
von Recklinghausenin neurofibromatoosi
-
von Recklinghausenin tauti
-
Swedish
URI
http://www.yso.fi/onto/mesh/D017253
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