Disease #04078 (CVID11 (immunodeficiency, variable, common, type 11 (CVID-11)), OMIM:615767)

Official abbreviation CVID11
Name immunodeficiency, variable, common, type 11 (CVID-11)
OMIM ID 615767
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IL21
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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