Disease #03351 (CVID6 (immunodeficiency, variable, common, type 6 (CVID-6)), OMIM:613496)

Official abbreviation CVID6
Name immunodeficiency, variable, common, type 6 (CVID-6)
OMIM ID 613496
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CD81
Associated tissues -
Disease features -
Remarks -

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