OBO ID: DOID:0081146
Term Name: common variable immunodeficiency 3 Search Ontology:
Synonyms:
Definition: A common variable immunodeficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CD19 gene on chromosome 16p11.2. https://pubmed.ncbi.nlm.nih.gov/16672701/
References:
Ontology: Human Disease   ( DOID:0081146 )
Relationships
is a type of:
OTHER common variable immunodeficiency 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CD19 Immunodeficiency, common variable, 3
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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