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: C4021998
Disease: Lack of skin elasticity
Lack of skin elasticity 		22 0 9 0.26 0 0
CUI: C4551630
Disease: Ichthyosis Congenita I
Ichthyosis Congenita I 		5 0 5 0.24 0 0
CUI: C0079583
Disease: Ichthyosiform Erythroderma, Congenital
Ichthyosiform Erythroderma, Congenital 		31 0 9 0.21 0 0
CUI: C1855789
Disease: Self-Healing Collodion Baby
Self-Healing Collodion Baby 		4 0 4 0.19 0 0
CUI: C3543867
Disease: Collodion Fetus
Collodion Fetus 		4 0 4 0.19 0 0
CUI: C0079154
Disease: Congenital Nonbullous Ichthyosiform Erythroderma
Congenital Nonbullous Ichthyosiform Erythroderma 		36 0 9 0.19 0 0
CUI: C3536797
Disease: Ichthyosis Congenita II
Ichthyosis Congenita II 		7 0 4 0.17 0 0
CUI: C0013592
Disease: Ectropion
Ectropion 		50 0 10 0.16 0 0
CUI: C4021956
Disease: Aplasia/Hypoplasia of the eyebrow
Aplasia/Hypoplasia of the eyebrow 		52 0 10 0.16 0 0
CUI: C1859235
Disease: Intrahepatic biliary dysgenesis
Intrahepatic biliary dysgenesis 		3 0 3 0.14 0 0
CUI: C3888093
Disease: ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 		3 0 3 0.14 0 0
CUI: C1866689
Disease: Short sacroiliac notch
Short sacroiliac notch 		4 0 3 0.14 0 0
CUI: C3550693
Disease: PEROXISOME BIOGENESIS DISORDER 3B
PEROXISOME BIOGENESIS DISORDER 3B 		5 0 3 0.13 0 0
CUI: C0853087
Disease: Nail abnormality
Nail abnormality 		67 0 10 0.13 0 0
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis 		16 0 4 0.12 0 0
CUI: C1850087
Disease: Narrow sacroiliac notch
Narrow sacroiliac notch 		7 0 3 0.12 0 0
CUI: C0011606
Disease: Exfoliative dermatitis
Exfoliative dermatitis 		64 0 9 0.12 0 0
CUI: C0221270
Disease: Acanthosis
Acanthosis 		37 0 6 0.12 0 0
CUI: C0017086
Disease: Gangrene
Gangrene 		69 0 9 0.11 0 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		69 0 9 0.11 0 0
CUI: C0432055
Disease: Simple syndactyly of fingers - first web
Simple syndactyly of fingers - first web 		9 0 3 0.11 0 0
CUI: C4721541
Disease: PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) 		11 0 3 0.10 0 0
CUI: C0392163
Disease: Corneal erosion
Corneal erosion 		33 0 5 0.10 0 0
CUI: C1274215
Disease: Autosomal recessive ichthyosis
Autosomal recessive ichthyosis 		2 0 2 9.5E-02 0 0
CUI: C1839277
Disease: Submucous cleft lip
Submucous cleft lip 		2 0 2 9.5E-02 0 0