Disease #03449 (C9D (complement component 9 deficiency (C9D)), OMIM:613825)
| Official abbreviation |
C9D |
| Name |
complement component 9 deficiency (C9D) |
| OMIM ID |
613825 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
C9 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2015-12-08 23:59:30 +01:00 (CET) |
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