Disease association ontology term - MONDO:0012146 - familial hemophagocytic lymphohistiocytosis 3
Term summary
- ID
- MONDO:0012146
- Name
- familial hemophagocytic lymphohistiocytosis 3
- Ontology or CV name
- Disease association
- Definition
- Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D gene.
