Search Ontology:
Human Disease

familial hemophagocytic lymphohistiocytosis 4

Term ID
DOID:0110924
Synonyms
  • FHL4
  • HLH4
  • HPLH4
Definition
A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the STX11 gene on chromosome 6q24.2. https://www.ncbi.nlm.nih.gov/pubmed/15703195
References
Ontology
Human Disease   ( DOID:0110924 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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