OBO ID: DOID:0081150 |
Term Name: | common variable immunodeficiency 7 | Search Ontology: | |
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Synonyms: |
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Definition: | A common variable immunodeficiency that has_material_basis_in compound heterozygous mutation in the CD21 gene (CR2) on chromosome 1q32. https://pubmed.ncbi.nlm.nih.gov/22035880/ | ||
References: | |||
Ontology: | Human Disease ( DOID:0081150 ) |
OTHER common variable immunodeficiency 7 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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CR2 | ?Immunodeficiency, common variable, 7 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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