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DO Term : familial hemophagocytic lymphohistiocytosis 1 [DOID:0110921] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the HPLH1 gene on chromosome 9q21.3-q22.
  • synonyms:
  • 267700,
  • HLH1,
  • HPLH1,
  • OMIM:267700,
  • FHL1
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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





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