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DOID:0090013 - severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive
Disease Ontology Definition:A severe combined immunodeficiency characterized by being T cell-negative, B cell-negative and natural killer cell-positive and that has_material_basis_in mutation in the RAG1 and RAG2 genes on chromosome 11p12.
Synonyms: SCID due to complete RAG1-2 deficiency, Severe combined immunodeficiency due to complete RAG1-2 deficiency, autosomal recessive T cell-negative, B-cell negative, NK cell-positive SCID,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0011086 - severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee