Search Ontology:
Human Disease
severe combined immunodeficiency with sensitivity to ionizing radiation
- Term ID
- DOID:0090012
- Synonyms
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- artemis deficiency
- SCID due to artemis deficiency
- SCID due to DCLRE1C deficiency
- SCID, Athabascan type
- SCID, Athabaskan type
- Severe combined immunodeficiency due to artemis deficiency
- Severe combined immunodeficiency due to DCLRE1C deficiency
- Severe combined immunodeficiency, Athabascan type
- Severe combined immunodeficiency, Athabaskan type
- Definition
- A severe combined immunodeficiency characterized by being T cell-negative, B cell-negative and natural killer cell-positive with sensitivity to ionizing radiation and that has_material_basis_in mutation in the DCLRE1C gene on chromosome 10p13. https://www.ncbi.nlm.nih.gov/pubmed/11336668
- References
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- ICD10CM:D81.1
- MESH:C537589
- MIM:602450
- ORDO:275
- Ontology
- Human Disease ( DOID:0090012 )
- is a type of
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Genes Involved
Zebrafish Models