C98934Level 8
Harlequin Ichthyosis
**Semantic type:** Disease or Syndrome
**Definition:** A very rare and usually lethal autosomal recessive inherited disorder of the skin caused by mutations in the ABCA12 gene. It is characterized by the presence of hard and thick skin. There are diamond-like plates formed in the skin which are separated by fissures.
GET
/api/v1/systems/nci_thesaurus/nodes/C98934Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.