World Of Taxonomy
C212036Level 5

Adrenomyeloneuropathy

**Semantic type:** Disease or Syndrome

**Definition:** A rare X-linked condition, caused by mutation(s) in the ABCD1 gene, encoding ATP-binding cassette sub-family D member 1. It may present with varying clinical findings and may present at different ages (child or adult).

GET/api/v1/systems/nci_thesaurus/nodes/C212036
Official DownloadCC BY 4.0Source

Hierarchy Explorer

Loading...

Cross-system equivalences0

No cross-system equivalences mapped for this node.