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: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.0E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 2.9E-02
CUI: C2750892
Disease: EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1
EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1 		0 2 0 0 1 2.9E-02
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 1.6E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 1.8E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.9E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.0E-03 0 0
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		138 0 1 2.0E-03 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead 		133 0 1 2.1E-03 0 0
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		131 0 1 2.1E-03 0 0
CUI: C0241355
Disease: Small testicle
Small testicle 		129 0 1 2.1E-03 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly 		127 0 1 2.1E-03 0 0
CUI: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism 		119 0 1 2.1E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 1 2.1E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 1 2.1E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 2.2E-03 0 0
CUI: C0426790
Disease: Narrow thorax
Narrow thorax 		112 0 1 2.2E-03 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair 		112 0 1 2.2E-03 0 0
CUI: C1835884
Disease: Triangular face
Triangular face 		111 0 1 2.2E-03 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 1 2.2E-03 0 0
CUI: C1843108
Disease: Short palm
Short palm 		110 0 1 2.2E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		109 0 1 2.2E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 2.2E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		101 0 1 2.2E-03 0 0
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		96 0 1 2.2E-03 0 0