Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 54 125 7.9E-02 13 0.10
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		213 83 134 8.4E-02 15 9.8E-02
CUI: C0949664
Disease: Tauopathies
Tauopathies 		245 43 155 9.7E-02 9 7.6E-02
CUI: C0542476
Disease: Forgetful
Forgetful 		429 18 257 0.15 7 7.3E-02
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		112 20 75 4.8E-02 7 7.1E-02
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease 		255 41 155 9.6E-02 8 6.8E-02
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		320 215 176 0.11 19 6.8E-02
CUI: C1504404
Disease: Hippocampal sclerosis
Hippocampal sclerosis 		84 14 50 3.2E-02 6 6.5E-02
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		978 115 473 0.23 12 6.4E-02
CUI: C0497327
Disease: Dementia
Dementia 		816 176 383 0.20 15 6.1E-02
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		718 159 349 0.19 14 6.1E-02
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 95 231 0.14 10 5.9E-02
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		607 47 332 0.19 7 5.6E-02
CUI: C0233794
Disease: Memory impairment
Memory impairment 		763 48 389 0.21 7 5.6E-02
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		1075 276 343 0.15 19 5.6E-02
CUI: C0233401
Disease: Psychiatric symptom
Psychiatric symptom 		95 12 55 3.5E-02 5 5.4E-02
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 32 31 2.0E-02 6 5.4E-02
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		83 20 51 3.3E-02 5 5.0E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		83 21 32 2.0E-02 5 5.0E-02
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		1263 112 416 0.18 9 4.8E-02
CUI: C0026837
Disease: Muscle Rigidity
Muscle Rigidity 		320 25 125 7.3E-02 5 4.8E-02
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		230 26 84 5.1E-02 5 4.7E-02
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 27 38 2.5E-02 5 4.7E-02
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		1 5 1 6.6E-04 4 4.7E-02
CUI: C1285162
Disease: Degenerative disorder
Degenerative disorder 		160 6 99 6.3E-02 4 4.6E-02