All diseases

OMIM ID
601321
OMIM term:
NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS
Alternative terms:
NOONAN-NEUROFIBROMATOSIS SYNDROME
NEUROFIBROMATOSIS WITH NOONAN PHENOTYPE
(∗) Location:
17q11.2  
(†) Associated OMIM genes:
NF1  
(‡) Associated MGI genes:

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