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: C0010678
Disease: Cysticercosis
Cysticercosis 		0 2 0 0 2 2.6E-02
CUI: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 1.3E-02
CUI: C0013505
Disease: Echinococcosis, Pulmonary
Echinococcosis, Pulmonary 		0 1 0 0 1 1.3E-02
CUI: C0265514
Disease: Dermatofibrosis lenticularis disseminata
Dermatofibrosis lenticularis disseminata 		0 3 0 0 1 1.3E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.6E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 2.6E-02
CUI: C0395887
Disease: Tympanosclerosis
Tympanosclerosis 		0 1 0 0 1 1.3E-02
CUI: C0948160
Disease: Pancreatic Infection
Pancreatic Infection 		0 1 0 0 1 1.3E-02
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO 		0 3 0 0 1 1.3E-02
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 1 2.4E-03 0 0
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		251 0 1 2.4E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 2.6E-03 0 0
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		593 0 2 2.7E-03 0 0
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		593 0 2 2.7E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.7E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 2.8E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 2.8E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 2.8E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 1 2.9E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 2.9E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 3.0E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 3.0E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 3.0E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 3.1E-03 0 0
CUI: C0042798
Disease: Low Vision
Low Vision 		157 0 1 3.2E-03 0 0