LAMC3, laminin subunit gamma 3, 10319

N. diseases: 30; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria
0.110 GeneticVariation disease BEFREE A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy. 29247375 2018
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria
0.110 Biomarker disease HPO