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Metadata
ID	DOID:0060588
Name	Noonan syndrome 10
Definition	A Noonan syndrome that has_material_basis_in heterozygous mutation in the LZTR1 gene on chromosome 22q11. https://www.ncbi.nlm.nih.gov/pubmed/25795793
Xrefs	ICD10CM:Q87.1 MIM:616564
Alternateids	DOID:0070110
Synonyms	NS10 [EXACT]
Parent Relationships	is_a Noonan syndrome is_a autosomal dominant disease