All diseases

OMIM ID
162200
OMIM term:
NEUROFIBROMATOSIS, TYPE I; NF1
Alternative terms:
NEUROFIBROMATOSIS, PERIPHERAL TYPE
VON RECKLINGHAUSEN DISEASE
(∗) Location:
17q11.2  
(†) Associated OMIM genes:
NF1  
(‡) Associated MGI genes:
Nf1   Trp53  

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