Disease #01832 (CGD-2 (granulomatous disease, chronic, due to deficiency of NCF-2, type 2), OMIM:233710)
| Official abbreviation |
CGD-2 |
| Name |
granulomatous disease, chronic, due to deficiency of NCF-2, type 2 |
| OMIM ID |
233710 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NCF2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
