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DO Term : immunodeficiency 13 [DOID:0111987] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A T cell deficiency characterized by decreased CD4 T-lymphocyte counts that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11.2.
  • synonyms:
  • UMLS_CUI:C3809768,
  • ICL,
  • OMIM:615518,
  • IMD13,
  • ORDO:228000,
  • idiopathic CD4 lymphopenia,
  • GARD:12375,
  • 615518
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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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