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: C0013927
Disease: Embolism, Amniotic Fluid
Embolism, Amniotic Fluid 		1 0 1 0.50 0 0
CUI: C0023052
Disease: Laryngeal Edema
Laryngeal Edema 		1 0 1 0.50 0 0
CUI: C0085659
Disease: Erythema marginatum
Erythema marginatum 		1 0 1 0.50 0 0
CUI: C0151610
Disease: Edema of the tongue
Edema of the tongue 		1 0 1 0.50 0 0
CUI: C0376704
Disease: Clinical Capillary Leak Syndrome
Clinical Capillary Leak Syndrome 		1 0 1 0.50 0 0
CUI: C0398775
Disease: Hereditary C1 esterase inhibitor deficiency - deficient factor
Hereditary C1 esterase inhibitor deficiency - deficient factor 		1 0 1 0.50 0 0
CUI: C0398776
Disease: Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor 		1 0 1 0.50 0 0
CUI: C0426601
Disease: Swallowing symptoms
Swallowing symptoms 		1 0 1 0.50 0 0
CUI: C0853619
Disease: Localized swelling
Localized swelling 		1 0 1 0.50 0 0
CUI: C1852700
Disease: Complement Component 4, Partial Deficiency Of
Complement Component 4, Partial Deficiency Of 		1 0 1 0.50 0 0
CUI: C4016986
Disease: COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR
COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF, DUE TO DYSFUNCTIONAL C1 INHIBITOR 		1 0 1 0.50 0 0
CUI: C4476719
Disease: Limbal edema
Limbal edema 		1 0 1 0.50 0 0
CUI: C4552030
Disease: Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus 		1 0 1 0.50 0 0
CUI: C4693994
Disease: CILIARY DYSKINESIA, PRIMARY, 7, WITH SITUS INVERSUS
CILIARY DYSKINESIA, PRIMARY, 7, WITH SITUS INVERSUS 		1 0 1 0.50 0 0
CUI: C0236024
Disease: Edema of pharynx
Edema of pharynx 		2 0 1 0.33 0 0
CUI: C0333240
Disease: Acute edema
Acute edema 		2 0 1 0.33 0 0
CUI: C1142262
Disease: Intestinal edema
Intestinal edema 		2 0 1 0.33 0 0
CUI: C1304177
Disease: Idiopathic angioedema
Idiopathic angioedema 		2 0 1 0.33 0 0
CUI: C1862892
Disease: Hereditary Angioedema Type II
Hereditary Angioedema Type II 		2 0 1 0.33 0 0
CUI: C2678473
Disease: CILIARY DYSKINESIA, PRIMARY, 7 (disorder)
CILIARY DYSKINESIA, PRIMARY, 7 (disorder) 		2 14 1 0.33 2 0.14
CUI: C2717905
Disease: Hereditary Angioedema Types I and II
Hereditary Angioedema Types I and II 		2 0 1 0.33 0 0
CUI: C2717906
Disease: Hereditary Angioedema Type I
Hereditary Angioedema Type I 		2 0 1 0.33 0 0
CUI: C3506079
Disease: Acquired C1 inhibitor deficiency
Acquired C1 inhibitor deficiency 		2 0 1 0.33 0 0
CUI: C4025190
Disease: Abnormal epiglottis morphology
Abnormal epiglottis morphology 		2 0 1 0.33 0 0
CUI: C0236116
Disease: SLE-like symptoms
SLE-like symptoms 		3 0 1 0.25 0 0