A Noonan syndrome that has_material_basis_in mutation in the RAF1 gene. [ url:https://www.ncbi.nlm.nih.gov/pubmed/17603483 http://purl.obolibrary.org/obo/ECO_0007645 ]

Synonyms: NS5

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:C548083
  • MIM:611553
  • ICD10CM:Q87.1
acronym
NS5

has alternative id

DOID:0070105

has obo namespace

disease_ontology

id

DOID:0060583