TSC2, TSC complex subunit 2, 7249

N. diseases: 410; N. variants: 317
Disease: Malformations of Cortical Development ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1955869
Disease: Malformations of Cortical Development
Malformations of Cortical Development 		0.010 Biomarker disease LHGDN Expression of tuberin and hamartin in tuberous sclerosis complex-associated and sporadic cortical dysplasia of Taylor's balloon cell type. 18368626 2008