A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/19966803 ]

Synonyms: NS6

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:C548084
  • MIM:613224
  • ICD10CM:Q87.1
acronym
NS6

has alternative id

DOID:0070106

has obo namespace

disease_ontology

id

DOID:0060584