C125697Level 5
Ehlers-Danlos Syndrome, Type II
**Semantic type:** Disease or Syndrome
**Definition:** A classic type of Ehlers-Danlos syndrome resulting from autosomal dominant mutation(s) in the COL5A2 gene, encoding collagen alpha-2(V) chain.
GET
/api/v1/systems/nci_thesaurus/nodes/C125697Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.