| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Developmental anomaly in which the vagina, bladder, and rectum fuse resulting in a common channel. (Human Phenotype Ontology, HP_0012621) |
| External Link | https://www.disgenet.org/browser/0/1/0/C0266225 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the disease Persistent Cloaca in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CDX2 | caudal type homeobox 2 |
