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: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis 		1 0 1 0.33 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 0.33 0 0
CUI: C1305147
Disease: Congenital supravalvular aortic stenosis
Congenital supravalvular aortic stenosis 		1 0 1 0.33 0 0
CUI: C3276539
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 1
CUTIS LAXA, AUTOSOMAL DOMINANT 1 		1 0 1 0.33 0 0
CUI: C3671688
Disease: Cyclic Hematopoesis
Cyclic Hematopoesis 		1 0 1 0.33 0 0
CUI: C3887897
Disease: Idiopathic atrophoderma of Pasini and Pierini
Idiopathic atrophoderma of Pasini and Pierini 		1 0 1 0.33 0 0
CUI: C4049241
Disease: Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency 		1 0 1 0.33 0 0
CUI: C4049455
Disease: Pseudoxanthoma elasticum-like papillary dermal elastolysis
Pseudoxanthoma elasticum-like papillary dermal elastolysis 		1 0 1 0.33 0 0
CUI: C4751167
Disease: Late-onset focal dermal elastosis
Late-onset focal dermal elastosis 		1 0 1 0.33 0 0
CUI: C0271407
Disease: Synchysis scintillans
Synchysis scintillans 		2 0 1 0.25 0 0
CUI: C1274789
Disease: Ligneous conjunctivitis
Ligneous conjunctivitis 		2 0 1 0.25 0 0
CUI: C1855792
Disease: ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1
ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1 		2 0 1 0.25 0 0
CUI: C3178892
Disease: Pelvic Floor Disorders
Pelvic Floor Disorders 		2 0 1 0.25 0 0
CUI: C3264562
Disease: Buried penis
Buried penis 		2 0 1 0.25 0 0
CUI: C4022392
Disease: Early onset of sexual maturation
Early onset of sexual maturation 		2 0 1 0.25 0 0
CUI: C4273756
Disease: Hepatoportal sclerosis
Hepatoportal sclerosis 		2 0 1 0.25 0 0
CUI: C0264220
Disease: Chronic disease of respiratory system
Chronic disease of respiratory system 		9 0 2 0.20 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant 		3 0 1 0.20 0 0
CUI: C0272175
Disease: Immune neutropenia
Immune neutropenia 		3 0 1 0.20 0 0
CUI: C0406549
Disease: Cutis laxa, acquired type
Cutis laxa, acquired type 		3 0 1 0.20 0 0
CUI: C0855999
Disease: Abnormal eosinophil morphology
Abnormal eosinophil morphology 		3 0 1 0.20 0 0
CUI: C1717804
Disease: Emphysema or COPD
Emphysema or COPD 		3 0 1 0.20 0 0
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		3 0 1 0.20 0 0
CUI: C1969833
Disease: COPD, Severe Early-Onset
COPD, Severe Early-Onset 		3 0 1 0.20 0 0
CUI: C2242658
Disease: Aortic dissection rupture
Aortic dissection rupture 		3 0 1 0.20 0 0