Disease #00053 (NS3 (Noonan syndrome 3), OMIM:609942)

Official abbreviation NS3
Name Noonan syndrome 3
OMIM ID 609942
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KRAS
Associated tissues -
Disease features -
Remarks -
Date created 2020-06-23 13:14:24 +00:00 (UTC)
Date last edited N/A

  Powered by LOVD v.3.0 Build 30
LOVD software ©2004-2024 Leiden University Medical Center 		There are currently no updates.