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: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 0.12
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 0.12
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 0.11
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.0E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 2 2.3E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 2.5E-03 0 0
CUI: C1136382
Disease: Sclerocystic Ovaries
Sclerocystic Ovaries 		144 0 1 2.7E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density 		138 0 1 2.7E-03 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		129 0 1 2.8E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.8E-03 0 0
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		126 0 1 2.8E-03 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis 		121 0 1 2.9E-03 0 0
CUI: C0236736
Disease: Cocaine-Related Disorders
Cocaine-Related Disorders 		121 0 1 2.9E-03 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia 		118 0 1 2.9E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 1 2.9E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 1 2.9E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 3.0E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 3.0E-03 0 0
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum 		105 0 1 3.0E-03 0 0
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain 		103 0 1 3.0E-03 0 0
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		102 0 1 3.0E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 3.1E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 3.1E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		94 0 1 3.1E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls 		94 0 1 3.1E-03 0 0