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DO Term : familial hemophagocytic lymphohistiocytosis 3 [DOID:0110923] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the UNC13D gene on chromosome 17q25.1.

synonyms:
HLH3,
OMIM:608898,
608898,
HPLH3,
FHL3,
GARD:9928

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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