Disease association ontology term - MONDO:0013135 - familial hemophagocytic lymphohistiocytosis 5
Term summary
- ID
- MONDO:0013135
- Name
- familial hemophagocytic lymphohistiocytosis 5
- Ontology or CV name
- Disease association
- Definition
- Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STXBP2 gene.
