Search Ontology:
Human Disease
immunodeficiency 26
- Term ID
- DOID:0111961
- Synonyms
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- 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
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- MIM:615966
- NCI:C176795
- ORDO:317425
- UMLS_CUI:C4014833
- Ontology
- Human Disease ( DOID:0111961 )
- is a type of
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Genes Involved
Zebrafish Models