motor aphasia Gene Set

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
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Genes

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