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: C0001726
Disease: Affective Symptoms
Affective Symptoms 		0 10 0 0 1 2.6E-03
CUI: C0036363
Disease: Schizotypal Personality Disorder
Schizotypal Personality Disorder 		0 9 0 0 1 2.6E-03
CUI: C0747249
Disease: Paranoid ideation
Paranoid ideation 		0 2 0 0 1 2.6E-03
CUI: C0006915
Disease: Caplan Syndrome
Caplan Syndrome 		1 0 1 6.0E-03 0 0
CUI: C0011548
Disease: Dependent Personality Disorder
Dependent Personality Disorder 		1 0 1 6.0E-03 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 6.0E-03 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 6.0E-03 0 0
CUI: C0024588
Disease: Malignant essential hypertension
Malignant essential hypertension 		1 0 1 6.0E-03 0 0
CUI: C0024967
Disease: Maximal Voluntary Ventilation
Maximal Voluntary Ventilation 		1 0 1 6.0E-03 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 6.0E-03 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 6.0E-03 0 0
CUI: C0035468
Disease: Rhinoscleroma
Rhinoscleroma 		1 0 1 6.0E-03 0 0
CUI: C0037768
Disease: Spasmophilia
Spasmophilia 		1 0 1 6.0E-03 0 0
CUI: C0040947
Disease: Trichostrongyloidiasis
Trichostrongyloidiasis 		1 0 1 6.0E-03 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 6.0E-03 0 0
CUI: C0153661
Disease: Malignant neoplasm of thorax
Malignant neoplasm of thorax 		1 0 1 6.0E-03 0 0
CUI: C0154628
Disease: Hyperkinetic conduct disorder of childhood
Hyperkinetic conduct disorder of childhood 		1 0 1 6.0E-03 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 6.0E-03 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 6.0E-03 0 0
CUI: C0267642
Disease: Childhood celiac disease
Childhood celiac disease 		1 0 1 6.0E-03 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 6.0E-03 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 6.0E-03 0 0
CUI: C0270224
Disease: Tetany, Neonatal
Tetany, Neonatal 		1 0 1 6.0E-03 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis 		1 0 1 6.0E-03 0 0
CUI: C0271198
Disease: Scotoma, Arcuate
Scotoma, Arcuate 		1 0 1 6.0E-03 0 0