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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