C84894Level 6
Monilethrix
**Semantic type:** Disease or Syndrome
**Definition:** A rare autosomal dominant inherited hair shaft disorder caused by mutations in certain cuticular type II keratin genes. It is characterized by the presence of thin, fragile hairs that appear beaded.
GET
/api/v1/systems/nci_thesaurus/nodes/C84894Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.