Metadata | |
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ID | DOID:0111957 |
Name | immunodeficiency 11A |
Definition | A severe combined immunodeficiency characterized by defective intracellular signaling in T and B cells, increased numbers of transitional B cells, hypogammaglobulinemia, decreased numbers of regulatory T cells and defects in T-cell function that has_material_basis_in homozygous or compound heterozygous mutation in the CARD11 gene on chromosome 7p22.2. https://pubmed.ncbi.nlm.nih.gov/23374270/, https://pubmed.ncbi.nlm.nih.gov/23561803/ |
Xrefs | |
Subsets |
DO_rare_slim |
Synonyms |
CARD11 deficiency [EXACT] IMD11A [EXACT] SCID due to CARD11 deficiency [EXACT] severe combined immunodeficiency due to CARD11 deficiency [EXACT] |
Parent Relationships |