OBO ID: DOID:0081153 |
Term Name: | common variable immunodeficiency 11 | Search Ontology: | |
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Definition: | A common variable immunodeficiency that has_material_basis_in homozygous mutation in the IL21 gene on chromosome 4q27. https://pubmed.ncbi.nlm.nih.gov/24746753/ | ||
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Ontology: | Human Disease ( DOID:0081153 ) |
OTHER common variable immunodeficiency 11 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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