Disease #04508 (IMD-27B (immunodeficiency, type 27B, mycobacteriosis, autosomal dominant (IMD-27B)), OMIM:615978)
| Official abbreviation |
IMD-27B |
| Name |
immunodeficiency, type 27B, mycobacteriosis, autosomal dominant (IMD-27B) |
| OMIM ID |
615978 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
IFNGR1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
N/A |
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