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: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 0.33
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA 		0 1 0 0 1 0.17
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 1 1.0E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		429 0 1 1.8E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 1 2.3E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 1 2.3E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 0 1 2.5E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.6E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 2.7E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		235 0 1 2.8E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 2.9E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.9E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 3.0E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 3.0E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 3.0E-03 0 0
CUI: C0005612
Disease: Birth Weight
Birth Weight 		214 0 1 3.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 3.1E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 0 1 3.2E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 3.2E-03 0 0
CUI: C1858085
Disease: Malar flattening
Malar flattening 		190 0 1 3.2E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 0 1 3.3E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 3.3E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 1 3.3E-03 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		182 0 1 3.3E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 3.3E-03 0 0