All diseases

OMIM ID
163950
OMIM term:
NOONAN SYNDROME 1; NS1
Alternative terms:
NOONAN SYNDROME
MALE TURNER SYNDROME
FEMALE PSEUDO-TURNER SYNDROME
TURNER PHENOTYPE WITH NORMAL KARYOTYPE PTERYGIUM COLLI SYNDROME, INCLUDED
(∗) Location:
12q24.13  
(†) Associated OMIM genes:
PTPN11  
(‡) Associated MGI genes:
Apaf1   Myst4   Ptpn11   Sos1  

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