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: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		226 0 1 3.5E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		218 0 1 3.6E-03 0 0
CUI: C0028960
Disease: Oligospermia
Oligospermia 		217 0 1 3.6E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		779 0 3 3.6E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		779 0 3 3.6E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 1 3.6E-03 0 0
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		486 0 2 3.6E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 1 3.6E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		477 0 2 3.7E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 1 3.7E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 3.8E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia 		453 0 2 3.9E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 3.9E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 3.9E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 1 4.0E-03 0 0
CUI: C1858085
Disease: Malar flattening
Malar flattening 		190 0 1 4.0E-03 0 0
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		190 0 1 4.0E-03 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		188 0 1 4.0E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 4.0E-03 0 0
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		433 0 2 4.0E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia 		184 0 1 4.0E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 1 4.1E-03 0 0
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		181 0 1 4.1E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 1 4.3E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		171 0 1 4.3E-03 0 0