RS121918463 PTPN11
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What This Variant Does
"[OMIM:?]
Associated Conditions
Noonan syndrome 1
Noonan syndrome
Early T cell progenitor acute lymphoblastic leukemia
RASopathy
Non-immune hydrops fetalis
Noonan syndrome and Noonan-related syndrome
Metachondromatosis
PTPN11-related disorder
LEOPARD syndrome 1
Pilocytic astrocytoma
RASopathy
Noonan syndrome
Noonan syndrome
RASopathy
Cardiovascular phenotype
Other Variants in PTPN11