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: C0349516
Disease: Isolated aortic stenosis
Isolated aortic stenosis 		3 0 1 3.7E-02 0 0
CUI: C0406587
Disease: Wrinkly skin syndrome
Wrinkly skin syndrome 		3 0 1 3.7E-02 0 0
CUI: C1261982
Disease: Chondrosis
Chondrosis 		3 0 1 3.7E-02 0 0
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		3 0 1 3.7E-02 0 0
CUI: C1840392
Disease: HYPERPIGMENTATION, FAMILIAL PROGRESSIVE
HYPERPIGMENTATION, FAMILIAL PROGRESSIVE 		3 0 1 3.7E-02 0 0
CUI: C1848459
Disease: High nonceruloplasmin-bound serum copper
High nonceruloplasmin-bound serum copper 		3 0 1 3.7E-02 0 0
CUI: C1861873
Disease: Multiple plantar creases
Multiple plantar creases 		3 0 1 3.7E-02 0 0
CUI: C2037047
Disease: Subretinal pigment epithelium hemorrhage
Subretinal pigment epithelium hemorrhage 		3 0 1 3.7E-02 0 0
CUI: C2675547
Disease: Slender long bones with narrow diaphyses
Slender long bones with narrow diaphyses 		3 0 1 3.7E-02 0 0
CUI: C2721646
Disease: Aneurysm enlargement
Aneurysm enlargement 		3 0 1 3.7E-02 0 0
CUI: C4087338
Disease: Mite allergy
Mite allergy 		3 0 1 3.7E-02 0 0
CUI: C4476553
Disease: Atrial septal dilatation
Atrial septal dilatation 		3 0 1 3.7E-02 0 0
CUI: C4476649
Disease: Abnormal apolipoprotein level
Abnormal apolipoprotein level 		3 0 1 3.7E-02 0 0
CUI: C4479387
Disease: CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC 		3 0 1 3.7E-02 0 0
CUI: C4479409
Disease: CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID 		3 0 1 3.7E-02 0 0
CUI: C0016427
Disease: Follicular cyst
Follicular cyst 		4 0 1 3.6E-02 0 0
CUI: C0353676
Disease: Organophosphorus Poisoning
Organophosphorus Poisoning 		4 0 1 3.6E-02 0 0
CUI: C0581366
Disease: Recurrent cystitis
Recurrent cystitis 		4 0 1 3.6E-02 0 0
CUI: C1851883
Disease: Small, conical teeth
Small, conical teeth 		4 0 1 3.6E-02 0 0
CUI: C1861872
Disease: Multiple palmar creases
Multiple palmar creases 		4 0 1 3.6E-02 0 0
CUI: C3494247
Disease: Organothiophosphonate Poisoning
Organothiophosphonate Poisoning 		4 0 1 3.6E-02 0 0
CUI: C3494248
Disease: Organothiophosphate Poisoning
Organothiophosphate Poisoning 		4 0 1 3.6E-02 0 0
CUI: C3662272
Disease: Drug pseudoallergy
Drug pseudoallergy 		4 0 1 3.6E-02 0 0
CUI: C4023610
Disease: Abnormality of the intrinsic pathway
Abnormality of the intrinsic pathway 		4 0 1 3.6E-02 0 0
CUI: C4024871
Disease: Prominent veins on trunk
Prominent veins on trunk 		4 0 1 3.6E-02 0 0