Search Ontology:
Human Disease

familial hemophagocytic lymphohistiocytosis 2

Term ID
DOID:0110922
Synonyms
  • FHL2
  • HLH2
  • HPLH2
Definition
A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the PRF1 gene on chromosome 10q22.1. https://www.ncbi.nlm.nih.gov/pubmed/10583959
References
Ontology
Human Disease   ( DOID:0110922 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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