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: C0949856
Disease: Oxidative Phosphorylation Deficiencies
Oxidative Phosphorylation Deficiencies 		18 0 9 0.47 0 0
CUI: C0949857
Disease: Mitochondrial Respiratory Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies 		49 0 9 0.18 0 0
CUI: C0242992
Disease: Multiple Chemical Sensitivity
Multiple Chemical Sensitivity 		5 0 2 0.15 0 0
CUI: C1527168
Disease: Bonnevie-Ullrich Syndrome
Bonnevie-Ullrich Syndrome 		5 0 2 0.15 0 0
CUI: C0395887
Disease: Tympanosclerosis
Tympanosclerosis 		7 0 2 0.13 0 0
CUI: C0475802
Disease: Perinatal anoxic-ischemic brain injury
Perinatal anoxic-ischemic brain injury 		7 0 2 0.13 0 0
CUI: C1837256
Disease: Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis 		9 0 2 0.12 0 0
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		21 0 3 0.11 0 0
CUI: C1850415
Disease: Microvesicular hepatic steatosis
Microvesicular hepatic steatosis 		11 0 2 0.11 0 0
CUI: C4721845
Disease: Marfan Syndrome, Type I
Marfan Syndrome, Type I 		11 0 2 0.11 0 0
CUI: C0033247
Disease: Proctocolitis
Proctocolitis 		1 0 1 1.0E-01 0 0
CUI: C0085740
Disease: Mendelson Syndrome
Mendelson Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0152497
Disease: Food poisoning caused by Vibrio parahaemolyticus
Food poisoning caused by Vibrio parahaemolyticus 		1 0 1 1.0E-01 0 0
CUI: C0206307
Disease: Canavan Disease
Canavan Disease 		12 0 2 1.0E-01 0 0
CUI: C0270975
Disease: Infantile encephalopathy AND lactic acidosis
Infantile encephalopathy AND lactic acidosis 		1 0 1 1.0E-01 0 0
CUI: C1510432
Disease: Radiation Sickness
Radiation Sickness 		1 0 1 1.0E-01 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 1.0E-01 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 1.0E-01 0 0
CUI: C1850407
Disease: Navajo Familial Neurogenic Arthropathy
Navajo Familial Neurogenic Arthropathy 		1 0 1 1.0E-01 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 1.0E-01 0 0
CUI: C2675128
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding) 		1 0 1 1.0E-01 0 0
CUI: C3539916
Disease: MYOCLONUS, FAMILIAL CORTICAL
MYOCLONUS, FAMILIAL CORTICAL 		1 0 1 1.0E-01 0 0
CUI: C3553374
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 5
COENZYME Q10 DEFICIENCY, PRIMARY, 5 		1 0 1 1.0E-01 0 0
CUI: C3825727
Disease: Respiratory allergy
Respiratory allergy 		1 0 1 1.0E-01 0 0
CUI: C4023055
Disease: Abnormality of central motor conduction
Abnormality of central motor conduction 		1 0 1 1.0E-01 0 0