C176931Level 6

Noonan Syndrome 3

**Semantic type:** Disease or Syndrome

**Definition:** Noonan syndrome caused by autosomal dominant mutation(s) in the KRAS gene, encoding GTPase KRas.

**Synonyms:** - NS3

GET/api/v1/systems/nci_thesaurus/nodes/C176931

Official DownloadCC BY 4.0Source

Hierarchy Explorer

No cross-system equivalences mapped for this node.

C176931 - Noonan Syndrome 3 - NCI Thesaurus - World Of Taxonomy | World Of Taxonomy