| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness. (Human Disease Ontology, DOID_4267) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0012672 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the akinetic mutism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SPG21 | spastic paraplegia 21 (autosomal recessive, Mast syndrome) |
