A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS2 gene on chromosome 14q21. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/25795793 ]

Synonyms: NS9

This is just here as a test because I lose it

Term information

database cross reference
  • MIM:616559
  • ICD10CM:Q87.1
acronym
NS9

has alternative id

DOID:0070109

has obo namespace

disease_ontology

id

DOID:0060587