C121564Level 6
Adenine Phosphoribosyltransferase Deficiency
**Semantic type:** Disease or Syndrome
**Definition:** An inherited condition caused by mutations in the APRT gene that affects the kidneys and urinary tract. The most common feature of this condition is recurrent kidney stones.
GET
/api/v1/systems/nci_thesaurus/nodes/C121564Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.