Chromosome 2p16.3 deletion syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| CHROMOSOME 2p16.3 DELETION SYNDROME | C3808494 | NRXN1 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |