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: C0239055
Disease: CHRONIC CRYPTOSPORIDIOSIS
CHRONIC CRYPTOSPORIDIOSIS 		1 0 1 0.17 0 0
CUI: C0282616
Disease: HIV Enteropathy
HIV Enteropathy 		1 0 1 0.17 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 0.17 0 0
CUI: C0746779
Disease: nausea chronic
nausea chronic 		1 0 1 0.17 0 0
CUI: C0752285
Disease: Hypersomnia, Post-Traumatic
Hypersomnia, Post-Traumatic 		1 0 1 0.17 0 0
CUI: C2675227
Disease: Endocrine-Cerebroosteodysplasia
Endocrine-Cerebroosteodysplasia 		1 0 1 0.17 0 0
CUI: C2750892
Disease: EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1
EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1 		1 0 1 0.17 0 0
CUI: C3697756
Disease: Chronic post-thoracotomy pain syndrome
Chronic post-thoracotomy pain syndrome 		1 0 1 0.17 0 0
CUI: C3854283
Disease: Pharyngeal dysphagia
Pharyngeal dysphagia 		1 0 1 0.17 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 0 1 0.17 0 0
CUI: C4023088
Disease: EEG with generalized polyspikes
EEG with generalized polyspikes 		1 0 1 0.17 0 0
CUI: C4025713
Disease: Paroxysmal drowsiness
Paroxysmal drowsiness 		1 0 1 0.17 0 0
CUI: C4509819
Disease: Endocrine-cerebro-osteodysplasia syndrome
Endocrine-cerebro-osteodysplasia syndrome 		1 0 1 0.17 0 0
CUI: C4693613
Disease: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10 		1 0 1 0.17 0 0
CUI: C0020524
Disease: Disorders of Excessive Somnolence
Disorders of Excessive Somnolence 		2 0 1 0.14 0 0
CUI: C0231813
Disease: Meningitic respiration
Meningitic respiration 		2 0 1 0.14 0 0
CUI: C0406299
Disease: Chronic prurigo
Chronic prurigo 		2 0 1 0.14 0 0
CUI: C0746668
Disease: muscle pain chronic
muscle pain chronic 		2 0 1 0.14 0 0
CUI: C0751137
Disease: Craniofacial Pain
Craniofacial Pain 		2 0 1 0.14 0 0
CUI: C1275421
Disease: Rapidly involuting congenital hemangioma
Rapidly involuting congenital hemangioma 		2 0 1 0.14 0 0
CUI: C1838192
Disease: SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder) 		2 0 1 0.14 0 0
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 0 1 0.14 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 0.14 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 1 0.14 0 0
CUI: C3697880
Disease: Intractable nausea and vomiting
Intractable nausea and vomiting 		2 0 1 0.14 0 0