MED13L, mediator complex subunit 13L, 23389

N. diseases: 94; N. variants: 49
Disease: Language Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023015
Disease: Language Disorders
Language Disorders 		0.010 GeneticVariation group BEFREE A prominent feature of the MED13L neurocognitive presentation is profound language impairment, often in combination with articulatory deficits. 25758992 2015