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: C0030193
Disease: Pain
Pain 		1554 196 305 0.13 10 1.7E-02
CUI: C0025958
Disease: Microcephaly
Microcephaly 		1064 0 246 0.13 0 0
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		560 179 185 0.12 10 1.8E-02
CUI: C0028754
Disease: Obesity
Obesity 		2821 1111 434 0.12 10 6.7E-03
CUI: C0013336
Disease: Dwarfism
Dwarfism 		1261 0 261 0.12 0 0
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		580 308 186 0.12 8 1.2E-02
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		607 47 188 0.12 1 2.3E-03
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		577 441 184 0.12 6 7.2E-03
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 226 0.12 12 1.2E-02
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		584 68 183 0.12 1 2.2E-03
CUI: C0349588
Disease: Short stature
Short stature 		1127 292 241 0.12 3 4.4E-03
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		560 192 178 0.12 14 2.4E-02
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		2509 386 384 0.12 7 9.0E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		3397 1843 477 0.12 16 7.2E-03
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		1010 0 224 0.12 0 0
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		2419 231 372 0.12 7 1.1E-02
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		2420 231 372 0.12 7 1.1E-02
CUI: C0497327
Disease: Dementia
Dementia 		816 176 203 0.12 10 1.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		2078 990 335 0.12 18 1.3E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		2322 1085 358 0.12 12 8.2E-03
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		1658 591 288 0.12 9 9.2E-03
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 73 227 0.11 4 8.6E-03
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		978 115 214 0.11 4 7.9E-03
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		1075 276 221 0.11 7 1.1E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		2359 710 344 0.11 9 8.2E-03