C125703Level 8
Fanconi Anemia, Complementation Group B
**Semantic type:** Disease or Syndrome
**Definition:** Fanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B.
GET
/api/v1/systems/nci_thesaurus/nodes/C125703Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.