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: C0730309
Disease: Inherited optic neuropathy
Inherited optic neuropathy 		1 0 1 5.3E-02 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 5.3E-02 0 0
CUI: C0751864
Disease: MPTP-Induced Degeneration of the Striatum
MPTP-Induced Degeneration of the Striatum 		1 0 1 5.3E-02 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 5.3E-02 0 0
CUI: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 5.3E-02 0 0
CUI: C1334557
Disease: Malignant Adult Brain Neoplasm
Malignant Adult Brain Neoplasm 		1 0 1 5.3E-02 0 0
CUI: C1513718
Disease: Mucin-Producing Intrahepatic Cholangiocarcinoma
Mucin-Producing Intrahepatic Cholangiocarcinoma 		1 0 1 5.3E-02 0 0
CUI: C1735375
Disease: Progressive optic neuropathy
Progressive optic neuropathy 		1 0 1 5.3E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 5.3E-02 0 0
CUI: C1833564
Disease: CONE-ROD DYSTROPHY 1 (disorder)
CONE-ROD DYSTROPHY 1 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C1841721
Disease: ACHROMATOPSIA 4
ACHROMATOPSIA 4 		1 0 1 5.3E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 5.3E-02 0 0
CUI: C1844776
Disease: CONE-ROD DYSTROPHY, X-LINKED, 1
CONE-ROD DYSTROPHY, X-LINKED, 1 		1 0 1 5.3E-02 0 0
CUI: C1852267
Disease: OPTIC ATROPHY 1 AND DEAFNESS
OPTIC ATROPHY 1 AND DEAFNESS 		1 0 1 5.3E-02 0 0
CUI: C1859524
Disease: Adductor longus contractures
Adductor longus contractures 		1 0 1 5.3E-02 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 5.3E-02 0 0
CUI: C1864900
Disease: Retinal Cone Dystrophy 3A
Retinal Cone Dystrophy 3A 		1 0 1 5.3E-02 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 5.3E-02 0 0
CUI: C2673931
Disease: Hyperthreoninuria
Hyperthreoninuria 		1 0 1 5.3E-02 0 0
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 0 1 5.3E-02 0 0
CUI: C2749137
Disease: Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness 		1 0 1 5.3E-02 0 0
CUI: C2751308
Disease: CONE DYSTROPHY 4 (disorder)
CONE DYSTROPHY 4 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C2751309
Disease: Achromatopsia 5
Achromatopsia 5 		1 0 1 5.3E-02 0 0