Search Ontology:
Human Disease

familial hemophagocytic lymphohistiocytosis 3

Term ID
DOID:0110923
Synonyms
  • FHL3
  • HLH3
  • HPLH3
Definition
A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the UNC13D gene on chromosome 17q25.1. https://www.ncbi.nlm.nih.gov/pubmed/14622600
References
Ontology
Human Disease   ( DOID:0110923 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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