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Metadata
ID	DOID:0060584
Name	Noonan syndrome 6
Definition	A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/19966803
Xrefs	ICD10CM:Q87.1 MESH:C548084 MIM:613224
Alternateids	DOID:0070106
Synonyms	NS6 [EXACT]
Parent Relationships	is_a Noonan syndrome is_a autosomal dominant disease