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: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 35 25 1.00 5 0.14
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 10 18 0.72 5 0.42
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 11 18 0.72 4 0.29
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome 		45 78 15 0.27 2 2.4E-02
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias 		29 0 9 0.20 0 0
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		4 0 4 0.16 0 0
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 12 0.14 0 0
CUI: C0266052
Disease: Precocious exfoliation of primary tooth
Precocious exfoliation of primary tooth 		20 0 5 0.12 0 0
CUI: C0021171
Disease: Bloch Sulzberger syndrome
Bloch Sulzberger syndrome 		41 0 7 0.12 0 0
CUI: C0265331
Disease: Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) 		4 0 3 0.12 0 0
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth 		14 0 4 0.11 0 0
CUI: C1844605
Disease: Periorbital wrinkles
Periorbital wrinkles 		5 0 3 0.11 0 0
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation 		5 0 3 0.11 0 0
CUI: C3665333
Disease: Keratitis-Ichthyosis-Deafness Syndrome
Keratitis-Ichthyosis-Deafness Syndrome 		5 12 3 0.11 1 5.6E-02
CUI: C0041972
Disease: Urethral Obstruction
Urethral Obstruction 		16 0 4 0.11 0 0
CUI: C1833225
Disease: Dystrophic toenail
Dystrophic toenail 		18 0 4 0.10 0 0
CUI: C0162361
Disease: Hidrotic Ectodermal Dysplasia
Hidrotic Ectodermal Dysplasia 		8 7 3 1.0E-01 1 7.7E-02
CUI: C0026265
Disease: Diseases of mitral valve
Diseases of mitral valve 		21 0 4 9.5E-02 0 0
CUI: C4023698
Disease: Everted upper lip vermilion
Everted upper lip vermilion 		12 0 3 8.8E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 3 8.6E-02 0 0
CUI: C3839753
Disease: Abnormality of nail of toe
Abnormality of nail of toe 		26 0 4 8.5E-02 0 0
CUI: C3551426
Disease: Dystrophic fingernails
Dystrophic fingernails 		27 0 4 8.3E-02 0 0
CUI: C0040427
Disease: Tooth Abnormalities
Tooth Abnormalities 		54 0 6 8.2E-02 0 0
CUI: C0399352
Disease: Developmental absence of tooth
Developmental absence of tooth 		41 0 5 8.2E-02 0 0
CUI: C0236053
Disease: Mucosal ulcer
Mucosal ulcer 		15 0 3 8.1E-02 0 0