| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Xref MGI. (Human Disease Ontology, DOID_8354) |
| External Link | http://www.omim.org/entry/613779 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the c3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| C3 | complement component 3 |
