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: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome 		45 78 25 0.51 1 1.3E-02
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 17 0.20 0 0
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 9 0.20 0 0
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 9 0.20 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 0.17 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 0.17 0 0
CUI: C0003028
Disease: Anhidrosis
Anhidrosis 		37 0 8 0.14 0 0
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		4 0 4 0.14 0 0
CUI: C0152915
Disease: Acute miliary tuberculosis
Acute miliary tuberculosis 		8 0 4 0.12 0 0
CUI: C0162361
Disease: Hidrotic Ectodermal Dysplasia
Hidrotic Ectodermal Dysplasia 		8 0 4 0.12 0 0
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		19 0 5 0.12 0 0
CUI: C0021171
Disease: Bloch Sulzberger syndrome
Bloch Sulzberger syndrome 		41 0 7 0.11 0 0
CUI: C4755296
Disease: Susceptibility to viral and mycobacterial infection
Susceptibility to viral and mycobacterial infection 		11 0 4 0.11 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		69 0 9 0.10 0 0
CUI: C0030105
Disease: Ozena (disorder)
Ozena (disorder) 		4 0 3 1.0E-01 0 0
CUI: C0265331
Disease: Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) 		4 0 3 1.0E-01 0 0
CUI: C0398795
Disease: Secondary immune deficiency disorder
Secondary immune deficiency disorder 		4 0 3 1.0E-01 0 0
CUI: C1844605
Disease: Periorbital wrinkles
Periorbital wrinkles 		5 0 3 9.7E-02 0 0
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation 		5 2 3 9.7E-02 1 0.33
CUI: C4082304
Disease: Oligodontia
Oligodontia 		62 34 8 9.6E-02 1 2.9E-02
CUI: C0266037
Disease: Peg-shaped teeth
Peg-shaped teeth 		17 2 4 9.5E-02 1 0.33
CUI: C2931027
Disease: Neutropenia, severe chronic
Neutropenia, severe chronic 		6 0 3 9.4E-02 0 0
CUI: C1833225
Disease: Dystrophic toenail
Dystrophic toenail 		18 0 4 9.3E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 6 9.1E-02 0 0
CUI: C0026919
Disease: Mycobacterium Infections, Nontuberculous
Mycobacterium Infections, Nontuberculous 		7 0 3 9.1E-02 0 0