Disease: Pachygyria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266483
Disease: Pachygyria
Pachygyria 		0.120 GeneticVariation disease BEFREE Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population. 31506600 2020
CUI: C0266483
Disease: Pachygyria
Pachygyria 		0.120 GeneticVariation disease BEFREE Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population. 30914828 2019
CUI: C0266483
Disease: Pachygyria
Pachygyria 		0.120 Biomarker disease HPO