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: C3151411
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
MENTAL RETARDATION, AUTOSOMAL DOMINANT 6 		1 0 1 0.50 0 0
CUI: C4015316
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27 		1 0 1 0.50 0 0
CUI: C1504541
Disease: Cerebellitis
Cerebellitis 		2 0 1 0.33 0 0
CUI: C0853946
Disease: Pain worsened
Pain worsened 		3 0 1 0.25 0 0
CUI: C0521686
Disease: Glaucomatous retinal degeneration
Glaucomatous retinal degeneration 		4 0 1 0.20 0 0
CUI: C0267509
Disease: Chronic idiopathic constipation
Chronic idiopathic constipation 		5 0 1 0.17 0 0
CUI: C0232491
Disease: Chronic abdominal pain
Chronic abdominal pain 		9 0 1 1.0E-01 0 0
CUI: C4268639
Disease: Irritable bowel syndrome with constipation
Irritable bowel syndrome with constipation 		11 0 1 8.3E-02 0 0
CUI: C0423673
Disease: Pain in spine
Pain in spine 		12 0 1 7.7E-02 0 0
CUI: C0679395
Disease: vascular ischemia
vascular ischemia 		12 0 1 7.7E-02 0 0
CUI: C0559469
Disease: Allergy to eggs
Allergy to eggs 		13 0 1 7.1E-02 0 0
CUI: C0007398
Disease: Catatonia
Catatonia 		14 0 1 6.7E-02 0 0
CUI: C0037316
Disease: Sleep Deprivation
Sleep Deprivation 		14 0 1 6.7E-02 0 0
CUI: C0158026
Disease: Monoarthritis
Monoarthritis 		14 0 1 6.7E-02 0 0
CUI: C1656427
Disease: Early onset schizophrenia
Early onset schizophrenia 		15 0 1 6.2E-02 0 0
CUI: C2931480
Disease: Neurofibromatosis, Type 3, mixed central and peripheral
Neurofibromatosis, Type 3, mixed central and peripheral 		15 0 1 6.2E-02 0 0
CUI: C0393702
Disease: Myoclonic Astatic Epilepsy
Myoclonic Astatic Epilepsy 		16 0 1 5.9E-02 0 0
CUI: C4023528
Disease: Abnormality of skin morphology
Abnormality of skin morphology 		16 0 1 5.9E-02 0 0
CUI: C0025221
Disease: Meleda Disease
Meleda Disease 		18 0 1 5.3E-02 0 0
CUI: C0267663
Disease: Congenital secretory diarrhea, sodium type (disorder)
Congenital secretory diarrhea, sodium type (disorder) 		18 0 1 5.3E-02 0 0
CUI: C0085625
Disease: Hypoalgesia
Hypoalgesia 		23 0 1 4.2E-02 0 0
CUI: C0563243
Disease: Poor coordination
Poor coordination 		26 0 1 3.7E-02 0 0
CUI: C1849718
Disease: POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE
POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE 		29 0 1 3.3E-02 0 0
CUI: C0234252
Disease: Mechanical pain
Mechanical pain 		30 0 1 3.2E-02 0 0
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		30 0 1 3.2E-02 0 0