C176902Level 9
Atypical Hemolytic Uremic Syndrome-4
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant subtype of atypical hemolytic uremic syndrome caused by mutation(s) in the CFB gene, encoding complement factor B.
**Synonyms:** - AHUS4
GET
/api/v1/systems/nci_thesaurus/nodes/C176902Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.