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: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 7.5E-03 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 7.5E-03 0 0
CUI: C0235328
Disease: Obstruction of colon
Obstruction of colon 		1 0 1 7.5E-03 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 7.5E-03 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia 		1 0 1 7.5E-03 0 0
CUI: C0267924
Disease: Suppurative cholangitis
Suppurative cholangitis 		1 0 1 7.5E-03 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism 		1 0 1 7.5E-03 0 0
CUI: C0398636
Disease: Acquired platelet disorder
Acquired platelet disorder 		1 0 1 7.5E-03 0 0
CUI: C0740905
Disease: allergy chronic
allergy chronic 		1 0 1 7.5E-03 0 0
CUI: C1275836
Disease: D - transposition of the great vessels
D - transposition of the great vessels 		1 0 1 7.5E-03 0 0
CUI: C1707332
Disease: Cellular Myxoma
Cellular Myxoma 		1 0 1 7.5E-03 0 0
CUI: C1709573
Disease: Pleural Epithelioid Hemangioendothelioma
Pleural Epithelioid Hemangioendothelioma 		1 0 1 7.5E-03 0 0
CUI: C1847711
Disease: NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO 		1 0 1 7.5E-03 0 0
CUI: C1848959
Disease: Mild eczema
Mild eczema 		1 0 1 7.5E-03 0 0
CUI: C1853949
Disease: MYASTHENIA, FAMILIAL INFANTILE, 1
MYASTHENIA, FAMILIAL INFANTILE, 1 		1 0 1 7.5E-03 0 0
CUI: C1861194
Disease: Thrombasthenia-Thrombocytopenia, Hereditary
Thrombasthenia-Thrombocytopenia, Hereditary 		1 0 1 7.5E-03 0 0
CUI: C1861863
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder) 		1 0 1 7.5E-03 0 0
CUI: C2675383
Disease: POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC
POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC 		1 0 1 7.5E-03 0 0
CUI: C2678476
Disease: Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Dilated, 1y 		1 0 1 7.5E-03 0 0
CUI: C2751259
Disease: Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related 		1 0 1 7.5E-03 0 0
CUI: C3149907
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 		1 0 1 7.5E-03 0 0
CUI: C3150700
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 20
MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 		1 0 1 7.5E-03 0 0
CUI: C3279422
Disease: Prominent incisors
Prominent incisors 		1 0 1 7.5E-03 0 0
CUI: C3279888
Disease: Frontal lobe atrophy
Frontal lobe atrophy 		1 0 1 7.5E-03 0 0
CUI: C3280120
Disease: Glycoprotein VI deficiency
Glycoprotein VI deficiency 		1 0 1 7.5E-03 0 0