16p13.2 deletion syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| 16p13.2 microdeletion syndrome | 500055 | USP7 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |
| CHROMOSOME 16p13.2 DELETION SYNDROME | C4225667 | USP7 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 26365382 | - |