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: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 2.6E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 2.6E-02 0 0
CUI: C0393560
Disease: Vascular Dementia, Acute Onset
Vascular Dementia, Acute Onset 		1 0 1 2.6E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 2.6E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 2.6E-02 0 0
CUI: C0600359
Disease: Arteriosclerotic Dementia
Arteriosclerotic Dementia 		1 0 1 2.6E-02 0 0
CUI: C1332860
Disease: Cauda Equina Paraganglioma
Cauda Equina Paraganglioma 		1 0 1 2.6E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 18 1 2.6E-02 1 5.3E-02
CUI: C1838818
Disease: MUSCLE STIFFNESS, PAINFUL
MUSCLE STIFFNESS, PAINFUL 		1 0 1 2.6E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 2.6E-02 0 0
CUI: C1868633
Disease: Paragangliomas with Sensorineural Hearing Loss
Paragangliomas with Sensorineural Hearing Loss 		1 0 1 2.6E-02 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 2.6E-02 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 0 1 2.6E-02 0 0
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG 		1 0 1 2.6E-02 0 0
CUI: C3151975
Disease: DEAFNESS, SENSORINEURAL, WITH NEUROLOGIC FEATURES
DEAFNESS, SENSORINEURAL, WITH NEUROLOGIC FEATURES 		1 0 1 2.6E-02 0 0
CUI: C3276074
Disease: PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS 		1 0 1 2.6E-02 0 0
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5 		1 0 1 2.6E-02 0 0
CUI: C3532243
Disease: Fatal infantile mitochondrial cardiomyopathy
Fatal infantile mitochondrial cardiomyopathy 		1 0 1 2.6E-02 0 0
CUI: C4015307
Disease: PERRAULT SYNDROME 5
PERRAULT SYNDROME 5 		1 0 1 2.6E-02 0 0
CUI: C4016270
Disease: CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC 		1 0 1 2.6E-02 0 0
CUI: C4016605
Disease: OPHTHALMOPLEGIA, ISOLATED
OPHTHALMOPLEGIA, ISOLATED 		1 0 1 2.6E-02 0 0
CUI: C4016615
Disease: CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY
CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY 		1 0 1 2.6E-02 0 0
CUI: C4016616
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH 		1 0 1 2.6E-02 0 0
CUI: C4016618
Disease: NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT
NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT 		1 0 1 2.6E-02 0 0
CUI: C4016626
Disease: MITOCHONDRIAL CYTOCHROME c OXIDASE DEFICIENCY
MITOCHONDRIAL CYTOCHROME c OXIDASE DEFICIENCY 		1 0 1 2.6E-02 0 0