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Disease association ontology term - MONDO:0011336 - familial hemophagocytic lymphohistiocytosis 4

Term summary

ID
MONDO:0011336
Name
familial hemophagocytic lymphohistiocytosis 4
Ontology or CV name
Disease association
Definition
Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STX11 gene.

Parents

Annotation

Disease association

MONDO:0011336 - familial hemophagocytic lymphohistiocytosis 4

References:

Genes: