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Metadata
ID DOID:0060587
Name Noonan syndrome 9
Definition A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS2 gene on chromosome 14q21.
https://www.ncbi.nlm.nih.gov/pubmed/25795793
Xrefs

ICD10CM:Q87.1

OMIM:616559

Alternateids

DOID:0070109

Synonyms

NS9 [EXACT]

Parent Relationships

is_a Noonan syndrome

is_a autosomal dominant disease

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