Disease #00053 (NS3 (Noonan syndrome 3), OMIM:609942)

Official abbreviation NS3
Name Noonan syndrome 3
OMIM ID 609942
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KRAS
Associated tissues -
Disease features -
Remarks -

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