Search Ontology:
Human Disease

familial hemophagocytic lymphohistiocytosis 5

Term ID
DOID:0110925
Synonyms
  • FHL5
  • HLH5
  • HPLH5
Definition
A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the STXBP2 gene on chromosome 19p13.2. https://www.ncbi.nlm.nih.gov/pubmed/19804848
References
Ontology
Human Disease   ( DOID:0110925 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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