Disease #02611 (HIGM3 (immunodeficiency, with hyper IgM, type 3 (HIGM-3)), OMIM:606843)
Official abbreviation |
HIGM3 |
Name |
immunodeficiency, with hyper IgM, type 3 (HIGM-3) |
OMIM ID |
606843 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CD40 |
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) |
Individuals
|