Search Ontology:
Human Disease

immunodeficiency 26

Term ID
DOID:0111961
Synonyms
  • IMD26
  • immunodeficiency 26, with or without neurologic abnormalities
  • SCID due to DNA-PKcs deficiency
  • severe combined immunodeficiency due to DNA-PKcs deficiency
Definition
A severe combined immunodeficiency characterized by virtually absent peripheral B and T cells but normal numbers of NK cells, complete block in B-cell differentiation, and a defect in slow repair of DNA double-strand breaks in fibroblasts, that has_material_basis_in homozygous or compound heterozygous mutation in the PRKDC gene on chromosome 8q11.21. (2)
References
  • MIM:615966
  • NCI:C176795
  • ORDO:317425
  • UMLS_CUI:C4014833
Ontology
Human Disease   ( DOID:0111961 )
Relationships
is a type of
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Genes Involved
Zebrafish Models