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: C0751784
Disease: Lafora Body Disease, Late Onset
Lafora Body Disease, Late Onset 		2 0 2 0.29 0 0
CUI: C1142223
Disease: Granulomatous iritis
Granulomatous iritis 		2 0 2 0.29 0 0
CUI: C1850764
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC 2B
EPILEPSY, PROGRESSIVE MYOCLONIC 2B 		2 0 2 0.29 0 0
CUI: C4317153
Disease: Simple partial occipital seizures
Simple partial occipital seizures 		2 0 2 0.29 0 0
CUI: C4476727
Disease: Erratic myoclonus
Erratic myoclonus 		3 0 2 0.25 0 0
CUI: C4706583
Disease: Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies
Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies 		3 0 2 0.25 0 0
CUI: C0751919
Disease: Acquired Neuromyotonia
Acquired Neuromyotonia 		4 0 2 0.22 0 0
CUI: C1849186
Disease: Severe photosensitivity
Severe photosensitivity 		4 0 2 0.22 0 0
CUI: C3806961
Disease: Giant somatosensory evoked potentials
Giant somatosensory evoked potentials 		4 0 2 0.22 0 0
CUI: C0917808
Disease: Vegetative State
Vegetative State 		5 0 2 0.20 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 0.14 0 0
CUI: C0234461
Disease: aphasic
aphasic 		1 0 1 0.14 0 0
CUI: C0271285
Disease: Epithelial basement membrane dystrophy
Epithelial basement membrane dystrophy 		1 0 1 0.14 0 0
CUI: C0339271
Disease: Salzmann nodular dystrophy
Salzmann nodular dystrophy 		1 0 1 0.14 0 0
CUI: C0454578
Disease: Receptive aphasia (finding)
Receptive aphasia (finding) 		1 0 1 0.14 0 0
CUI: C0521723
Disease: Corneal dystrophy, epithelial basement membrane
Corneal dystrophy, epithelial basement membrane 		1 0 1 0.14 0 0
CUI: C1272765
Disease: Minimal deviation adenocarcinoma of endocervical type
Minimal deviation adenocarcinoma of endocervical type 		1 0 1 0.14 0 0
CUI: C1641846
Disease: Groenouw corneal dystrophy type I (disorder)
Groenouw corneal dystrophy type I (disorder) 		1 0 1 0.14 0 0
CUI: C1837974
Disease: Corneal Dystrophy, Lattice Type IIIA
Corneal Dystrophy, Lattice Type IIIA 		1 0 1 0.14 0 0
CUI: C3496177
Disease: Atypical psychosis
Atypical psychosis 		1 0 1 0.14 0 0
CUI: C3809374
Disease: EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5 		1 0 1 0.14 0 0
CUI: C4024792
Disease: Nodular corneal dystrophy
Nodular corneal dystrophy 		1 0 1 0.14 0 0
CUI: C4024796
Disease: Punctate corneal dystrophy
Punctate corneal dystrophy 		1 0 1 0.14 0 0
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		10 0 2 0.13 0 0
CUI: C0010035
Disease: Hereditary corneal dystrophy
Hereditary corneal dystrophy 		2 0 1 0.12 0 0