| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A speech disorder that involves a complete inability to speak. (Human Disease Ontology, DOID_4189) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D009155 |
| Similar Terms | |
| Downloads & Tools |
7 genes/proteins associated with the disease Mutism from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| PRL | prolactin | 1.28364 |
| ABCB1 | ATP-binding cassette, sub-family B (MDR/TAP), member 1 | 1.12426 |
| MAPK3 | mitogen-activated protein kinase 3 | 1.08019 |
| MAPK1 | mitogen-activated protein kinase 1 | 1.07411 |
| IL6 | interleukin 6 | 1.07163 |
| NR3C1 | nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) | 1.04904 |
| AVP | arginine vasopressin | 1.04757 |
