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: C1843792
Disease: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED 		0.980 Biomarker disease CTD_human
CUI: C1843792
Disease: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED 		0.980 Biomarker disease GENOMICS_ENGLAND
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		0.900 CausalMutation disease CLINVAR
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		0.900 Biomarker disease HPO
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		0.900 GeneticVariation disease CLINVAR
CUI: C3539123
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 11
CEROID LIPOFUSCINOSIS, NEURONAL, 11 		0.700 Biomarker disease CTD_human
CUI: C3539123
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 11
CEROID LIPOFUSCINOSIS, NEURONAL, 11 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3539123
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 11
CEROID LIPOFUSCINOSIS, NEURONAL, 11 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0497327
Disease: Dementia
Dementia 		0.500 Biomarker disease HPO
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.400 Biomarker disease HPO
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
Primary Progressive Aphasia (disorder) 		0.400 CausalMutation disease CLINVAR
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.300 Biomarker group GENOMICS_ENGLAND
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.300 Biomarker group GENOMICS_ENGLAND
CUI: C1850792
Disease: Congenital myasthenic syndrome ib
Congenital myasthenic syndrome ib 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.200 GeneticVariation disease CLINVAR
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.200 Biomarker group HPO
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		0.180 Biomarker disease HPO
CUI: C4551584
Disease: Brain atrophy
Brain atrophy 		0.170 Biomarker disease HPO
CUI: C0233794
Disease: Memory impairment
Memory impairment 		0.140 Biomarker phenotype HPO
CUI: C0003467
Disease: Anxiety
Anxiety 		0.120 Biomarker disease HPO
CUI: C0003537
Disease: Aphasia
Aphasia 		0.120 Biomarker disease HPO
CUI: C0003635
Disease: Apraxias
Apraxias 		0.120 Biomarker group HPO
CUI: C0085632
Disease: Apathy
Apathy 		0.120 Biomarker phenotype HPO
CUI: C0003113
Disease: Anomia
Anomia 		0.110 Biomarker disease HPO
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.110 Biomarker group HPO