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: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 0.50
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA 		0 1 0 0 1 0.25
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 0 1 2.3E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.5E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 2 2.7E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 2.8E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.9E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.9E-03 0 0
CUI: C0008489
Disease: Chorea
Chorea 		168 0 1 2.9E-03 0 0
CUI: C0023380
Disease: Lethargy
Lethargy 		160 0 1 3.0E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		160 0 1 3.0E-03 0 0
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		483 0 2 3.1E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		152 0 1 3.1E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 3.1E-03 0 0
CUI: C0424678
Disease: Lean body mass
Lean body mass 		144 0 1 3.2E-03 0 0
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		138 0 1 3.2E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 3.3E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 2 3.3E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 3.3E-03 0 0
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		126 0 1 3.3E-03 0 0
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		126 0 1 3.3E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 3.4E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 3.4E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 3.4E-03 0 0
CUI: C0039070
Disease: Syncope
Syncope 		119 0 1 3.4E-03 0 0