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: C4015067
Disease: AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS 		2 0 2 0.12 0 0
CUI: C4518562
Disease: Pneumonia caused by Gram positive bacteria
Pneumonia caused by Gram positive bacteria 		5 0 2 0.11 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 2 9.5E-02 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 2 8.3E-02 0 0
CUI: C0022504
Disease: Kaposi Varicelliform Eruption
Kaposi Varicelliform Eruption 		1 0 1 6.2E-02 0 0
CUI: C0030975
Disease: Perceptual Disorders
Perceptual Disorders 		1 0 1 6.2E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 6.2E-02 0 0
CUI: C0796089
Disease: LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE
LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE 		1 0 1 6.2E-02 0 0
CUI: C0854498
Disease: Muscular sarcoidosis
Muscular sarcoidosis 		1 0 1 6.2E-02 0 0
CUI: C1285175
Disease: Autoimmune connective tissue disorder
Autoimmune connective tissue disorder 		1 0 1 6.2E-02 0 0
CUI: C1829648
Disease: Amino acidemias
Amino acidemias 		1 0 1 6.2E-02 0 0
CUI: C2887627
Disease: Chronic sialoadenitis
Chronic sialoadenitis 		1 0 1 6.2E-02 0 0
CUI: C4015276
Disease: FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4 		1 0 1 6.2E-02 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 0 1 6.2E-02 0 0
CUI: C4017280
Disease: HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY
HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY 		1 0 1 6.2E-02 0 0
CUI: C4225327
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		1 0 1 6.2E-02 0 0
CUI: C0157742
Disease: Urticaria due to cold and heat
Urticaria due to cold and heat 		2 0 1 5.9E-02 0 0
CUI: C1838192
Disease: SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder) 		2 0 1 5.9E-02 0 0
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 0 1 5.9E-02 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 5.9E-02 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 1 5.9E-02 0 0
CUI: C4025600
Disease: Reduced xanthine dehydrogenase activity
Reduced xanthine dehydrogenase activity 		2 0 1 5.9E-02 0 0
CUI: C0021192
Disease: Indeterminate leprosy
Indeterminate leprosy 		3 0 1 5.6E-02 0 0
CUI: C0220988
Disease: Xanthinuria
Xanthinuria 		3 0 1 5.6E-02 0 0
CUI: C0268120
Disease: Adenine phosphoribosyltransferase deficiency
Adenine phosphoribosyltransferase deficiency 		3 0 1 5.6E-02 0 0