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: C1846496
Disease: Gaze Palsy, Familial Horizontal, with Progressive Scoliosis
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 		3 0 3 1.00 0 0
CUI: C4024794
Disease: Horizontal supranuclear gaze palsy
Horizontal supranuclear gaze palsy 		3 0 2 0.50 0 0
CUI: C0017570
Disease: Gingival Neoplasms
Gingival Neoplasms 		1 0 1 0.33 0 0
CUI: C0339651
Disease: Horizontal gaze palsy
Horizontal gaze palsy 		1 1 1 0.33 1 9.1E-02
CUI: C4015970
Disease: ESOPHAGEAL CARCINOMA, SOMATIC
ESOPHAGEAL CARCINOMA, SOMATIC 		1 0 1 0.33 0 0
CUI: C4479640
Disease: GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 		1 0 1 0.33 0 0
CUI: C1832215
Disease: Athabaskan brainstem dysgenesis
Athabaskan brainstem dysgenesis 		2 0 1 0.25 0 0
CUI: C1832216
Disease: Bosley-Salih-Alorainy Syndrome
Bosley-Salih-Alorainy Syndrome 		2 0 1 0.25 0 0
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1 		2 0 1 0.25 0 0
CUI: C3179058
Disease: Corpus Callosum Malformation
Corpus Callosum Malformation 		2 0 1 0.25 0 0
CUI: C0429702
Disease: Respiratory quotient
Respiratory quotient 		3 0 1 0.20 0 0
CUI: C2062713
Disease: Progressive ophthalmoplegia
Progressive ophthalmoplegia 		3 0 1 0.20 0 0
CUI: C3898473
Disease: Malignant biliary obstruction
Malignant biliary obstruction 		3 0 1 0.20 0 0
CUI: C4021520
Disease: Abnormal cerebral artery morphology
Abnormal cerebral artery morphology 		3 0 1 0.20 0 0
CUI: C0858005
Disease: Influenza B virus infection
Influenza B virus infection 		5 0 1 0.14 0 0
CUI: C4025704
Disease: Abnormality of the corticospinal tract
Abnormality of the corticospinal tract 		5 0 1 0.14 0 0
CUI: C4476591
Disease: Dysgenesis of the hippocampus
Dysgenesis of the hippocampus 		5 0 1 0.14 0 0
CUI: C0153942
Disease: Benign neoplasm of esophagus
Benign neoplasm of esophagus 		6 0 1 0.12 0 0
CUI: C0154059
Disease: Carcinoma in situ of esophagus
Carcinoma in situ of esophagus 		6 0 1 0.12 0 0
CUI: C1832932
Disease: DEAFNESS, AUTOSOMAL DOMINANT 5 (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 5 (disorder) 		6 0 1 0.12 0 0
CUI: C4225380
Disease: SINGLETON-MERTEN SYNDROME 2
SINGLETON-MERTEN SYNDROME 2 		6 0 1 0.12 0 0
CUI: C0220664
Disease: BRACHYDACTYLY, TYPE D
BRACHYDACTYLY, TYPE D 		8 0 1 1.0E-01 0 0
CUI: C0432254
Disease: Singleton Merten syndrome
Singleton Merten syndrome 		8 0 1 1.0E-01 0 0
CUI: C0019097
Disease: Hemorrhagic Fever, Argentinian
Hemorrhagic Fever, Argentinian 		9 0 1 9.1E-02 0 0
CUI: C0205671
Disease: Infections, Arenavirus
Infections, Arenavirus 		12 0 1 7.1E-02 0 0