|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|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.
|GJB1||gap junction protein, beta 1, 32kDa|