NLGN3, neuroligin 3, 54413

N. diseases: 63; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction
0.010 GeneticVariation phenotype BEFREE Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3. 31119867 2019