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: C0278608
Disease: Adult Liposarcoma
Adult Liposarcoma 		143 0 1 2.9E-03 0 0
CUI: C0279984
Disease: Childhood Liposarcoma
Childhood Liposarcoma 		143 0 1 2.9E-03 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum 		138 0 1 2.9E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 1 2.9E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 3.0E-03 0 0
CUI: C0021359
Disease: Infertility
Infertility 		130 0 1 3.0E-03 0 0
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		129 0 1 3.0E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 1 3.0E-03 0 0
CUI: C0855197
Disease: Malignant Testicular Germ Cell Tumor
Malignant Testicular Germ Cell Tumor 		128 0 1 3.0E-03 0 0
CUI: C1328407
Disease: Hip Dysplasia
Hip Dysplasia 		128 0 1 3.0E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		127 0 1 3.0E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 3.1E-03 0 0
CUI: C0236736
Disease: Cocaine-Related Disorders
Cocaine-Related Disorders 		121 0 1 3.1E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes 		121 0 1 3.1E-03 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		118 0 1 3.1E-03 0 0
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		117 0 1 3.1E-03 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 0 2 3.2E-03 0 0
CUI: C1306710
Disease: Facial asymmetry
Facial asymmetry 		109 0 1 3.2E-03 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0 		109 0 1 3.2E-03 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0 		108 0 1 3.2E-03 0 0
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		105 0 1 3.2E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 3.2E-03 0 0
CUI: C4552100
Disease: Lynch Syndrome
Lynch Syndrome 		103 0 1 3.3E-03 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 2 3.3E-03 0 0
CUI: C0279592
Disease: Adult T Acute Lymphoblastic Leukemia
Adult T Acute Lymphoblastic Leukemia 		102 0 1 3.3E-03 0 0