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: C4551957
Disease: Epilepsy, Familial Temporal Lobe 1
Epilepsy, Familial Temporal Lobe 1 		7 0 1 0.14 0 0
CUI: C1838062
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Lateral Temporal Lobe Epilepsy 		8 0 1 0.12 0 0
CUI: C0391958
Disease: Familial Epilepsies
Familial Epilepsies 		16 0 1 6.2E-02 0 0
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis 		27 0 1 3.7E-02 0 0
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal 		29 0 1 3.4E-02 0 0
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes 		46 0 1 2.2E-02 0 0
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		95 0 1 1.1E-02 0 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		96 0 1 1.0E-02 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 9.4E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 8.9E-03 0 0
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis 		135 0 1 7.4E-03 0 0
CUI: C0751295
Disease: Memory Loss
Memory Loss 		163 0 1 6.1E-03 0 0
CUI: C0002622
Disease: Amnesia
Amnesia 		173 0 1 5.8E-03 0 0
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		183 0 1 5.5E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 5.3E-03 0 0
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
Hypertrophic obstructive cardiomyopathy 		233 0 1 4.3E-03 0 0
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
Classical Hodgkin's Lymphoma 		285 0 1 3.5E-03 0 0
CUI: C4552766
Disease: Miscarriage
Miscarriage 		426 0 1 2.3E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		477 0 1 2.1E-03 0 0
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		480 0 1 2.1E-03 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		497 0 1 2.0E-03 0 0
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		560 0 1 1.8E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 0 1 1.8E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 0 1 1.7E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		955 0 1 1.0E-03 0 0