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: C4025740
Disease: Autoamputation of foot
Autoamputation of foot 		2 0 2 0.33 0 0
CUI: C1855772
Disease: Absent corpus callosum cataract immunodeficiency
Absent corpus callosum cataract immunodeficiency 		4 0 2 0.25 0 0
CUI: C0086405
Disease: Hereditary Sensory Radicular Neuropathy
Hereditary Sensory Radicular Neuropathy 		5 0 2 0.22 0 0
CUI: C4049342
Disease: Foot osteomyelitis
Foot osteomyelitis 		5 0 2 0.22 0 0
CUI: C0234229
Disease: Deep pain
Deep pain 		1 0 1 0.17 0 0
CUI: C0346363
Disease: Nevus of conjunctiva
Nevus of conjunctiva 		1 0 1 0.17 0 0
CUI: C0403639
Disease: Chemical cystitis
Chemical cystitis 		1 0 1 0.17 0 0
CUI: C1319183
Disease: Corticosteroid induced cataract
Corticosteroid induced cataract 		1 0 1 0.17 0 0
CUI: C1697976
Disease: Hypotestosteronism
Hypotestosteronism 		1 0 1 0.17 0 0
CUI: C1847902
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder) 		1 0 1 0.17 0 0
CUI: C3280203
Disease: WARBURG MICRO SYNDROME 3
WARBURG MICRO SYNDROME 3 		1 0 1 0.17 0 0
CUI: C3809272
Disease: LETHAL CONGENITAL CONTRACTURE SYNDROME 5
LETHAL CONGENITAL CONTRACTURE SYNDROME 5 		1 0 1 0.17 0 0
CUI: C3854438
Disease: Rapidly progressive osteoarthritis
Rapidly progressive osteoarthritis 		1 0 1 0.17 0 0
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome 		16 0 3 0.16 0 0
CUI: C2936797
Disease: Acid cholesteryl ester hydrolase deficiency, type 2
Acid cholesteryl ester hydrolase deficiency, type 2 		9 0 2 0.15 0 0
CUI: C0027889
Disease: Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Autonomic Neuropathies 		25 0 4 0.15 0 0
CUI: C0432066
Disease: Congenital malformation syndromes affecting facial appearance
Congenital malformation syndromes affecting facial appearance 		2 0 1 0.14 0 0
CUI: C1096253
Disease: Cardiac infection
Cardiac infection 		2 0 1 0.14 0 0
CUI: C1842237
Disease: Charcot-Marie-Tooth Disease, Dominant Intermediate C
Charcot-Marie-Tooth Disease, Dominant Intermediate C 		2 0 1 0.14 0 0
CUI: C4024916
Disease: Decreased number of small peripheral myelinated nerve fibers
Decreased number of small peripheral myelinated nerve fibers 		2 0 1 0.14 0 0
CUI: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary 		19 0 3 0.14 0 0
CUI: C0423747
Disease: Deep pain on intercourse
Deep pain on intercourse 		3 0 1 0.12 0 0
CUI: C0687154
Disease: Acrocephalopolysyndactyly
Acrocephalopolysyndactyly 		3 0 1 0.12 0 0
CUI: C4025214
Disease: Sleepy facial expression
Sleepy facial expression 		3 0 1 0.12 0 0
CUI: C4050314
Disease: ROSE Cluster 3
ROSE Cluster 3 		3 0 1 0.12 0 0