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: C0008445
Disease: Chondrodysplasia Punctata
Chondrodysplasia Punctata 		16 0 6 0.35 0 0
CUI: C0263627
Disease: Calcinosis universalis
Calcinosis universalis 		2 0 2 0.29 0 0
CUI: C3669395
Disease: X-Linked Chondrodysplasia Punctata 1
X-Linked Chondrodysplasia Punctata 1 		2 0 2 0.29 0 0
CUI: C0282102
Disease: Chondrodysplasia punctata, X-linked dominant type
Chondrodysplasia punctata, X-linked dominant type 		9 0 3 0.23 0 0
CUI: C0265374
Disease: Warfarin syndrome
Warfarin syndrome 		4 0 2 0.22 0 0
CUI: C0265267
Disease: Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 		6 0 2 0.18 0 0
CUI: C0270709
Disease: Rud Syndrome
Rud Syndrome 		1 0 1 0.14 0 0
CUI: C0333662
Disease: Hemiatrophy
Hemiatrophy 		1 0 1 0.14 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 0.14 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 0.14 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 0.14 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 0.14 0 0
CUI: C0853241
Disease: Exacerbation of anxiety
Exacerbation of anxiety 		1 0 1 0.14 0 0
CUI: C1304147
Disease: Retention hyperkeratosis
Retention hyperkeratosis 		1 0 1 0.14 0 0
CUI: C1840013
Disease: Elevated 8-dehydrocholesterol
Elevated 8-dehydrocholesterol 		1 0 1 0.14 0 0
CUI: C1840014
Disease: Elevated 8(9)-cholestenol
Elevated 8(9)-cholestenol 		1 0 1 0.14 0 0
CUI: C1844846
Disease: Stippled calcification in carpal bones
Stippled calcification in carpal bones 		1 0 1 0.14 0 0
CUI: C1844848
Disease: Tarsal stippling
Tarsal stippling 		1 0 1 0.14 0 0
CUI: C2610861
Disease: 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase activity
2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase activity 		1 0 1 0.14 0 0
CUI: C3151781
Disease: CK syndrome
CK syndrome 		1 0 1 0.14 0 0
CUI: C4016464
Disease: CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT, ATYPICAL
CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT, ATYPICAL 		1 0 1 0.14 0 0
CUI: C4024153
Disease: Asymmetry of the mouth
Asymmetry of the mouth 		1 0 1 0.14 0 0
CUI: C4274085
Disease: Syndromic recessive X-linked ichthyosis
Syndromic recessive X-linked ichthyosis 		1 0 1 0.14 0 0
CUI: C4512053
Disease: 4p16.3 microduplication syndrome
4p16.3 microduplication syndrome 		1 0 1 0.14 0 0
CUI: C4520921
Disease: Stage 0 Gastric Cancer AJCC v6 and v7
Stage 0 Gastric Cancer AJCC v6 and v7 		1 0 1 0.14 0 0