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: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 7.7E-02 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 7.7E-02 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration 		1 0 1 7.7E-02 0 0
CUI: C0334635
Disease: Malignant lymphoma - centrocytic
Malignant lymphoma - centrocytic 		1 0 1 7.7E-02 0 0
CUI: C0334636
Disease: Malignant lymphoma, mixed small and large cell, diffuse
Malignant lymphoma, mixed small and large cell, diffuse 		1 0 1 7.7E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 7.7E-02 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect 		1 0 1 7.7E-02 0 0
CUI: C0855036
Disease: Alveolar soft part sarcoma metastatic
Alveolar soft part sarcoma metastatic 		1 0 1 7.7E-02 0 0
CUI: C0860452
Disease: Loss of skin elasticity
Loss of skin elasticity 		1 0 1 7.7E-02 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait 		1 0 1 7.7E-02 0 0
CUI: C1290309
Disease: Neoplasm of chest wall
Neoplasm of chest wall 		1 0 1 7.7E-02 0 0
CUI: C1336749
Disease: Thyroid Diffuse Large B-Cell Lymphoma
Thyroid Diffuse Large B-Cell Lymphoma 		1 0 1 7.7E-02 0 0
CUI: C1608971
Disease: Optic nerve pallor
Optic nerve pallor 		1 0 1 7.7E-02 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia 		1 0 1 7.7E-02 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex 		1 0 1 7.7E-02 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 7.7E-02 0 0
CUI: C1850309
Disease: Mildly elevated creatine phosphokinase
Mildly elevated creatine phosphokinase 		1 1 1 7.7E-02 1 0.25
CUI: C1857747
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder) 		1 0 1 7.7E-02 0 0
CUI: C2750220
Disease: Karak Syndrome
Karak Syndrome 		1 0 1 7.7E-02 0 0
CUI: C3553816
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13 		1 0 1 7.7E-02 0 0
CUI: C4020920
Disease: Enlarged interhemispheric fissure
Enlarged interhemispheric fissure 		1 0 1 7.7E-02 0 0
CUI: C4022743
Disease: T2 hypointense basal ganglia
T2 hypointense basal ganglia 		1 0 1 7.7E-02 0 0
CUI: C4022768
Disease: Cerebellar gliosis
Cerebellar gliosis 		1 0 1 7.7E-02 0 0
CUI: C4023074
Disease: EEG with parietal focal spikes
EEG with parietal focal spikes 		1 1 1 7.7E-02 1 0.25
CUI: C4023405
Disease: Abnormality of ocular abduction
Abnormality of ocular abduction 		1 0 1 7.7E-02 0 0