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DO Term : familial hemophagocytic lymphohistiocytosis 5 [DOID:0110925] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the STXBP2 gene on chromosome 19p13.2.
  • synonyms:
  • 613101,
  • FHL5,
  • HLH5,
  • OMIM:613101,
  • HPLH5
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents