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: C1856660
Disease: Abnormality of the helix
Abnormality of the helix 		21 0 9 0.11 0 0
CUI: C0011606
Disease: Exfoliative dermatitis
Exfoliative dermatitis 		64 0 13 0.11 0 0
CUI: C0151908
Disease: Dry skin
Dry skin 		159 0 22 0.11 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 0 20 0.11 0 0
CUI: C0079154
Disease: Congenital Nonbullous Ichthyosiform Erythroderma
Congenital Nonbullous Ichthyosiform Erythroderma 		36 0 10 0.11 0 0
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis 		176 0 23 0.10 0 0
CUI: C0013592
Disease: Ectropion
Ectropion 		50 0 11 0.10 0 0
CUI: C1853246
Disease: Eversion of lower lip
Eversion of lower lip 		105 0 16 0.10 0 0
CUI: C0431448
Disease: Absent eyebrow
Absent eyebrow 		19 0 8 1.0E-01 0 0
CUI: C0020758
Disease: Congenital ichthyosis
Congenital ichthyosis 		80 0 13 9.6E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 375 48 9.4E-02 1 2.7E-03
CUI: C4551675
Disease: Keratoderma, Palmoplantar
Keratoderma, Palmoplantar 		165 0 20 9.3E-02 0 0
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth 		14 0 7 9.2E-02 0 0
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis 		16 0 7 9.0E-02 0 0
CUI: C0423757
Disease: Thin skin
Thin skin 		77 0 12 9.0E-02 0 0
CUI: C0263383
Disease: Keratosis pilaris
Keratosis pilaris 		30 0 8 8.8E-02 0 0
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 0 7 8.7E-02 0 0
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 0 7 8.7E-02 0 0
CUI: C0033774
Disease: Pruritus
Pruritus 		107 0 14 8.6E-02 0 0
CUI: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic 		57 0 10 8.6E-02 0 0
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome 		45 0 9 8.6E-02 0 0
CUI: C0392163
Disease: Corneal erosion
Corneal erosion 		33 0 8 8.5E-02 0 0
CUI: C0237849
Disease: Peeling of skin
Peeling of skin 		21 0 7 8.4E-02 0 0
CUI: C4082304
Disease: Oligodontia
Oligodontia 		62 0 10 8.3E-02 0 0
CUI: C0003028
Disease: Anhidrosis
Anhidrosis 		37 0 8 8.2E-02 0 0