OBO ID: DOID:0081152 |
Term Name: | common variable immunodeficiency 10 | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24. https://pubmed.ncbi.nlm.nih.gov/24140114/ | ||
References: | |||
Ontology: | Human Disease ( DOID:0081152 ) |
OTHER common variable immunodeficiency 10 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.