[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. ( CSP )]
UMLS (CSP) C0162678 Relation/PAR: Genetic Condition
Familiar Neoplastic Syndrome
Neurofibroma
Neurocutaneous Syndromes
Heredodegenerative Disorders, Nervous System
Relation/CHD: Neurofibromatosis 1
acoustic neurofibromatosis