| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Impairment of expressive language and relative preservation of receptive language abilities. That is, the patient understands language (speech, writing) but cannot express it. (Human Phenotype Ontology, HP_0002427) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0002427 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the motor aphasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GJB1 | gap junction protein, beta 1, 32kDa |
