Disease #06300 (IMD52 (Immunodeficiency, type 52), OMIM:617514)
| Official abbreviation |
IMD52 |
| Name |
Immunodeficiency, type 52 |
| OMIM ID |
617514 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
LAT |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2022-05-23 16:58:44 +02:00 (CEST) |
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