Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 158038
Gene Symbol: LINGO2
LINGO2
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		0.010 GeneticVariation BEFREE Here we report a de novo genomic microdeletion that includes the LINGO2 gene as well as two microRNA genes, MIR873 and MIR876, in a patient with craniofacial abnormalities - in particular macrocephaly and hypertelorism - and learning difficulties. 25680557

2015