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: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly 		85 0 1 1.2E-03 0 0
CUI: C0002880
Disease: Autoimmune hemolytic anemia
Autoimmune hemolytic anemia 		81 0 1 1.3E-03 0 0
CUI: C0039128
Disease: Syphilis
Syphilis 		80 0 1 1.3E-03 0 0
CUI: C0236733
Disease: Amphetamine-Related Disorders
Amphetamine-Related Disorders 		78 0 1 1.3E-03 0 0
CUI: C0236807
Disease: Amphetamine Abuse
Amphetamine Abuse 		75 0 1 1.3E-03 0 0
CUI: C3160814
Disease: Cannabis use
Cannabis use 		74 0 1 1.3E-03 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure 		73 0 1 1.3E-03 0 0
CUI: C0343284
Disease: Chondrodysplasia
Chondrodysplasia 		71 0 1 1.3E-03 0 0
CUI: C0023364
Disease: Leptospirosis
Leptospirosis 		70 0 1 1.3E-03 0 0
CUI: C0042693
Disease: Violence
Violence 		70 0 1 1.3E-03 0 0
CUI: C0014121
Disease: Bacterial Endocarditis
Bacterial Endocarditis 		68 0 1 1.3E-03 0 0
CUI: C0156149
Disease: Gastrointestinal tract vascular insufficiency
Gastrointestinal tract vascular insufficiency 		68 0 1 1.3E-03 0 0
CUI: C2004435
Disease: Vascular insufficiency of intestine
Vascular insufficiency of intestine 		68 0 1 1.3E-03 0 0
CUI: C0021122
Disease: Disruptive, Impulse Control, and Conduct Disorders
Disruptive, Impulse Control, and Conduct Disorders 		67 0 1 1.3E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 1.3E-03 0 0
CUI: C0030807
Disease: Pemphigus
Pemphigus 		67 0 1 1.3E-03 0 0
CUI: C0853087
Disease: Nail abnormality
Nail abnormality 		67 0 1 1.3E-03 0 0
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		67 0 1 1.3E-03 0 0
CUI: C1849193
Disease: PEELING SKIN SYNDROME
PEELING SKIN SYNDROME 		67 0 1 1.3E-03 0 0
CUI: C0155094
Disease: Corneal pannus
Corneal pannus 		66 0 1 1.3E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 1.3E-03 0 0
CUI: C0003165
Disease: Anthracosis
Anthracosis 		65 0 1 1.3E-03 0 0
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		65 0 1 1.3E-03 0 0
CUI: C1832588
Disease: Chromosome 11p11.2 Deletion Syndrome
Chromosome 11p11.2 Deletion Syndrome 		65 0 1 1.3E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 1.3E-03 0 0