Gene: C9orf72 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.110 GeneticVariation group BEFREE In the neuropsychological assessment, C9orf72 mutated patients differed from non-mutated for the high frequency of visuospatial dysfunction regarding constructional apraxia (p = 0.02). 25285776 2015
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.110 Biomarker group HPO