A Noonan syndrome that has_material_basis_in heterozygous mutation in the KRAS gene. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/16474405 ]

Synonyms: NS3

This is just here as a test because I lose it

Term information

database cross reference
  • MIM:609942
  • ICD10CM:Q87.1
  • MESH:C537847
acronym
NS3

has alternative id

DOID:0070103

has obo namespace

disease_ontology

id

DOID:0060581