NRXN1, neurexin 1, 9378

N. diseases: 139; N. variants: 41
Disease: Specific language impairment ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		0.020 GeneticVariation disease BEFREE Disruption of a number of these genes (including NRXN1, CNTNAP2 and CASK) are known to cause diverse neurodevelopmental brain disorder phenotypes including schizophenia, autism, learning disability and specific language disorder. 20574149 2011
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		0.020 Biomarker disease BEFREE At a gene level, CAM genes associated in all three samples (NRXN1 and CNTNAP2), which were previously implicated in specific language disorder, autism and schizophrenia. 20157312 2011