|OBO ID: DOID:0060580|
|Term Name:||Noonan syndrome 2||Search Ontology:|
|Definition:||A Noonan syndrome characterized by hypertrophic obstructive cardiomyopathy and that has_material_basis_in an autosomal recessive inheritance. https://www.ncbi.nlm.nih.gov/pubmed/5782826|
|Ontology:||Human Disease (DOID:0060580)|
|is a type of:||
OTHER Noonan syndrome 2 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.