| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| P2RX1 | purinergic receptor P2X, ligand gated ion channel, 1 |
