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DO Term : immunodeficiency 38 [DOID:0111934] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A primary immunodeficiency disease characterized by development of severe clinical disease upon infection with weakly virulent mycobacteria and intracranial calcification that has_material_basis_in homozygous or compound heterozygous mutation in the ISG15 gene on chromosome 1p36.33.
  • synonyms:
  • OMIM:616126,
  • autosomal recessive ISG15 deficiency,
  • Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency,
  • immunodeficiency 38, mycobacteriosis, autosomal recessive,
  • immunodeficiency 38 with basal ganglia calcification,
  • ORDO:319563,
  • 616126,
  • IMD38
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents