UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
N N- N0 N3 NA NB NC ND NE NF NG NH NI NK NL NM NN NO NP NR NS NT NU NV NX NY NZ
NE NE- NEA NEB NEC NED NEE NEF NEG NEI NEL NEM NEN NEO NEP NER NES NET NEU NEV NEW NEX NEZ

neurofibromatoses

[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
 
Neoplastic Process
Relation/PAR: Genetic Condition
Familiar Neoplastic Syndrome
Neurofibroma
Neurocutaneous Syndromes
Heredodegenerative Disorders, Nervous System
Relation/CHD: Neurofibromatosis 1
acoustic neurofibromatosis

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