GRN, granulin precursor, 2896

N. diseases: 412; N. variants: 66
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003537
Disease: Aphasia
Aphasia
0.120 GeneticVariation disease BEFREE The clinical presentation of the GRN A9D missense mutation is not restricted to behavioral variant frontotemporal dementia and may include aphasia, extrapyramidal features, and, notably, amyotrophic lateral sclerosis. 23596077 2013
CUI: C0003537
Disease: Aphasia
Aphasia
0.120 GeneticVariation disease BEFREE Here we undertook a systematic study of nonverbal sound processing in patient groups with canonical dementia syndromes comprising clinically diagnosed typical amnestic Alzheimer's disease (AD; n=21), progressive nonfluent aphasia (PNFA; n=5), logopenic progressive aphasia (LPA; n=7) and aphasia in association with a progranulin gene mutation (GAA; n=1), and in healthy age-matched controls (n=20). 21689671 2011
CUI: C0003537
Disease: Aphasia
Aphasia
0.120 Biomarker disease HPO