Search Ontology:
Human Disease

familial hemophagocytic lymphohistiocytosis 1

Term ID
DOID:0110921
Synonyms
  • FHL1
  • HLH1
  • HPLH1
Definition
A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the HPLH1 gene on chromosome 9q21.3-q22. https://www.ncbi.nlm.nih.gov/pubmed/9915955
References
Ontology
Human Disease   ( DOID:0110921 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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