C128802Level 6
Acrodermatitis Enteropathica
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal recessive genetic disorder caused by mutations in the SLC39A4 gene, encoding zinc transporter ZIP4. The condition is characterized by zinc deficiency, periorificial and acral dermatitis, and diarrhea.
GET
/api/v1/systems/nci_thesaurus/nodes/C128802Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.