A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS1 gene on chromosome 2p22. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/19438935 ]

Synonyms: NS4

This is just here as a test because I lose it

Term information

database cross reference
  • MIM:610733
  • ICD10CM:Q87.1
  • MESH:C548082
acronym
NS4

has alternative id

DOID:0070104

has obo namespace

disease_ontology

id

DOID:0060582