LAMA1, laminin subunit alpha 1, 284217

N. diseases: 107; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027092
Disease: Myopia
Myopia
0.110 GeneticVariation disease BEFREE Cystic cerebellar dysplasia and biallelic LAMA1 mutations: a lamininopathy associated with tics, obsessive compulsive traits and myopia due to cell adhesion and migration defects. 27095636 2016
CUI: C0027092
Disease: Myopia
Myopia
0.110 Biomarker disease HPO
CUI: C0027092
Disease: Myopia
Myopia
0.110 CausalMutation disease CLINVAR