OBO ID: DOID:0112169
Term Name: Noonan syndrome 11 Search Ontology:
Synonyms:
  • NS11
Definition: A Noonan syndrome characterized by clinical characteristics of Noonan syndrome, varying impairment of intellectual development, and cardiac hypertrophy that has_material_basis_in heterozygous mutation in the MRAS gene on chromosome 3q22.3. https://pubmed.ncbi.nlm.nih.gov/28289718/
References:
Ontology: Human Disease   ( DOID:0112169 )
OTHER Noonan syndrome 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MRAS Noonan syndrome 11 618499
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None