World Of Taxonomy
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/C84894
Official DownloadCC BY 4.0Source

Hierarchy Explorer

Loading...

Cross-system equivalences0

No cross-system equivalences mapped for this node.