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: C0033931
Disease: Psychophysiologic Disorders
Psychophysiologic Disorders 		1 0 1 4.2E-02 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 4.2E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 4.2E-02 0 0
CUI: C0234505
Disease: Tactile Agnosia
Tactile Agnosia 		1 0 1 4.2E-02 0 0
CUI: C0334635
Disease: Malignant lymphoma - centrocytic
Malignant lymphoma - centrocytic 		1 0 1 4.2E-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 4.2E-02 0 0
CUI: C0338900
Disease: Psychasthenic neurosis
Psychasthenic neurosis 		1 0 1 4.2E-02 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 4.2E-02 0 0
CUI: C0542165
Disease: Pseudoparkinsonism
Pseudoparkinsonism 		1 0 1 4.2E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 4.2E-02 0 0
CUI: C0848200
Disease: Afterbirth pain
Afterbirth pain 		1 0 1 4.2E-02 0 0
CUI: C0855036
Disease: Alveolar soft part sarcoma metastatic
Alveolar soft part sarcoma metastatic 		1 0 1 4.2E-02 0 0
CUI: C0860452
Disease: Loss of skin elasticity
Loss of skin elasticity 		1 0 1 4.2E-02 0 0
CUI: C1274520
Disease: Fixed cutaneous sporotrichosis
Fixed cutaneous sporotrichosis 		1 0 1 4.2E-02 0 0
CUI: C1290309
Disease: Neoplasm of chest wall
Neoplasm of chest wall 		1 0 1 4.2E-02 0 0
CUI: C1328618
Disease: Agraphesthesia
Agraphesthesia 		1 0 1 4.2E-02 0 0
CUI: C1336749
Disease: Thyroid Diffuse Large B-Cell Lymphoma
Thyroid Diffuse Large B-Cell Lymphoma 		1 0 1 4.2E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 4.2E-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 0 1 4.2E-02 0 0
CUI: C1836460
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 		1 0 1 4.2E-02 0 0
CUI: C1837154
Disease: Drug Metabolism, Poor, CYP2D6-Related
Drug Metabolism, Poor, CYP2D6-Related 		1 0 1 4.2E-02 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 4.2E-02 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 4.2E-02 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 4.2E-02 0 0
CUI: C1843632
Disease: LEPROSY, SUSCEPTIBILITY TO, 2
LEPROSY, SUSCEPTIBILITY TO, 2 		1 0 1 4.2E-02 0 0