OBO ID: DOID:0110922
Term Name: familial hemophagocytic lymphohistiocytosis 2 Search Ontology:
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 familial hemophagocytic lymphohistiocytosis 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PRF1 Hemophagocytic lymphohistiocytosis, familial, 2
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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