RS121918466 PTPN11
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What This Variant Does
"[OMIM:?]
Associated Conditions
Noonan syndrome 1
Noonan syndrome
RASopathy
LEOPARD syndrome 1
Metachondromatosis
Juvenile myelomonocytic leukemia
Noonan syndrome 3
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
PTPN11-related disorder
Monogenic short statue
Congenital portosystemic shunt
RASopathy
Noonan syndrome 1
Noonan syndrome
Other Variants in PTPN11