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: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 14 6.9E-02 0 0
CUI: C0221292
Disease: Basophilic leukemia
Basophilic leukemia 		32 0 6 6.8E-02 0 0
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy 		17 0 5 6.8E-02 0 0
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome 		194 0 16 6.7E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		18 0 5 6.7E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 5 6.7E-02 0 0
CUI: C0085632
Disease: Apathy
Apathy 		83 0 9 6.6E-02 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis 		19 0 5 6.6E-02 0 0
CUI: C4042861
Disease: Obesity, Metabolically Benign
Obesity, Metabolically Benign 		19 0 5 6.6E-02 0 0
CUI: C0543859
Disease: Amyotrophic Lateral Sclerosis, Guam Form
Amyotrophic Lateral Sclerosis, Guam Form 		36 0 6 6.5E-02 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive 		5 0 4 6.3E-02 0 0
CUI: C3840049
Disease: Dysexecutive syndrome
Dysexecutive syndrome 		5 0 4 6.3E-02 0 0
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		173 0 14 6.3E-02 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		22 0 5 6.3E-02 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 5 6.2E-02 0 0
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		213 0 16 6.2E-02 0 0
CUI: C0039496
Disease: Temporomandibular Joint Dysfunction Syndrome
Temporomandibular Joint Dysfunction Syndrome 		24 0 5 6.2E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 8 6.2E-02 0 0
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		320 0 22 6.1E-02 0 0
CUI: C0263661
Disease: Disorder of skeletal system
Disorder of skeletal system 		25 0 5 6.1E-02 0 0
CUI: C0233401
Disease: Psychiatric symptom
Psychiatric symptom 		95 0 9 6.1E-02 0 0
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		130 0 11 6.1E-02 0 0
CUI: C1260881
Disease: Allergic bronchitis
Allergic bronchitis 		8 0 4 6.1E-02 0 0
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		61 0 7 6.0E-02 0 0
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 4 6.0E-02 0 0