Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Dermatofibrosis lenticularis disseminata
0 3 0 0 1 2.2E-03
Respiratory syncytial virus bronchiolitis
0 1 0 0 1 2.2E-03
CUI: C0947912
Disease: Myasthenias
Myasthenias
0 3 0 0 1 2.2E-03
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
272 0 1 1.6E-03 0 0
CUI: C4317109
Disease: Epileptic Seizures
Epileptic Seizures
250 0 1 1.7E-03 0 0
Creatine phosphokinase serum increased
228 0 1 1.8E-03 0 0
CUI: C0264716
Disease: Chronic heart failure
Chronic heart failure
223 0 1 1.8E-03 0 0
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders
218 0 1 1.8E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 1 1.8E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion
211 0 1 1.8E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
210 0 1 1.8E-03 0 0
CUI: C0270824
Disease: Visual seizure
Visual seizure
209 0 1 1.8E-03 0 0
CUI: C0035204
Disease: Respiration Disorders
Respiration Disorders
208 0 1 1.8E-03 0 0
CUI: C0150055
Disease: Chronic pain
Chronic pain
207 0 1 1.8E-03 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
194 269 1 1.9E-03 1 1.4E-03
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
192 0 1 1.9E-03 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection
192 0 1 1.9E-03 0 0
CUI: C0035243
Disease: Respiratory Tract Infections
Respiratory Tract Infections
187 0 1 1.9E-03 0 0
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
185 0 1 1.9E-03 0 0
CUI: C0740858
Disease: Substance abuse problem
Substance abuse problem
185 0 1 1.9E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 1 1.9E-03 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
182 0 1 1.9E-03 0 0
Small for gestational age (disorder)
181 0 1 1.9E-03 0 0
CUI: C0029882
Disease: Otitis Media
Otitis Media
175 0 1 2.0E-03 0 0
Amyotrophic Lateral Sclerosis, Sporadic
173 0 1 2.0E-03 0 0