Disease #02744 (IMD73A (immunodeficiency, type 73A, with defective neutrophil chemotaxix and leukocytosis), OMIM:608203)
| Official abbreviation |
IMD73A |
| Name |
immunodeficiency, type 73A, with defective neutrophil chemotaxix and leukocytosis |
| OMIM ID |
608203 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
RAC2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-07-29 11:51:53 +02:00 (CEST) |
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