Helsmoortel-van der aa syndrome
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder | C4014538 | ADNP | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 24531329, 25169753, 25294932 | - |