MeSH Browser

MeSH Heading: Neurofibromatoses
Tree Number(s): C04.557.580.600.580.590; C04.700.631; C10.562.600; C10.574.500.549; C16.320.400.560; C16.320.700.633
Unique ID: D017253
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D017253
Annotation: 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)
Entry Term(s): Multiple Neurofibromas; Neurofibromatosis; Neurofibromatosis 3; Neurofibromatosis Syndrome; Neurofibromatosis Type 3
NLM Classification #: QZ 380
Public MeSH Note: 2000; see NEUROFIBROMATOSIS 1993-1999
History Note: 2000(1993)
Date Established: 1993/01/01
Date of Entry: 1992/05/22
Revision Date: 2018/06/29

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0026175
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)
Terms: Neurofibromatoses Preferred Term
Term UI T051431
Date05/02/1992
LexicalTag NON
ThesaurusID NLM (1993); Multiple Neurofibromas
Term UI T372069
Date11/03/1999
LexicalTag NON
ThesaurusID NLM (2000); Neurofibromatosis
Term UI T051432
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1993); Neurofibromatosis Syndrome
Term UI T372777
Date11/03/1999
LexicalTag NON
ThesaurusID NLM (2000)

Neurofibromatoses MeSH Descriptor Data 2024