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Metadata
ID	DOID:0060581
Name	Noonan syndrome 3
Definition	A Noonan syndrome that has_material_basis_in heterozygous mutation in the KRAS gene. https://www.ncbi.nlm.nih.gov/pubmed/16474405
Xrefs	ICD10CM:Q87.1 MESH:C537847 OMIM:609942
Alternateids	DOID:0070103
Synonyms	NS3 [EXACT]
Parent Relationships	is_a Noonan syndrome is_a autosomal dominant disease