A Noonan syndrome that has_material_basis_in heterozygous mutation in the LZTR1 gene on chromosome 22q11. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/25795793 ]

Synonyms: NS10

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10CM:Q87.1
  • MIM:616564
acronym
NS10

has alternative id

DOID:0070110

has obo namespace

disease_ontology

id

DOID:0060588