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: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 11 18 1.00 4 0.24
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 7 18 0.72 5 0.42
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 35 18 0.72 9 0.25
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		4 0 4 0.22 0 0
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias 		29 0 7 0.17 0 0
CUI: C0265331
Disease: Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) 		4 0 3 0.16 0 0
CUI: C0266052
Disease: Precocious exfoliation of primary tooth
Precocious exfoliation of primary tooth 		20 0 5 0.15 0 0
CUI: C1844605
Disease: Periorbital wrinkles
Periorbital wrinkles 		5 0 3 0.15 0 0
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation 		5 0 3 0.15 0 0
CUI: C3665333
Disease: Keratitis-Ichthyosis-Deafness Syndrome
Keratitis-Ichthyosis-Deafness Syndrome 		5 12 3 0.15 1 4.8E-02
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome 		45 78 8 0.15 2 2.3E-02
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth 		14 0 4 0.14 0 0
CUI: C0021171
Disease: Bloch Sulzberger syndrome
Bloch Sulzberger syndrome 		41 0 6 0.11 0 0
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 9 0.11 0 0
CUI: C1720965
Disease: Ectodermal Dysplasia 3, Anhidrotic
Ectodermal Dysplasia 3, Anhidrotic 		2 0 2 0.11 0 0
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b 		2 16 2 0.11 1 4.0E-02
CUI: C4023698
Disease: Everted upper lip vermilion
Everted upper lip vermilion 		12 0 3 0.11 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 3 0.11 0 0
CUI: C2673760
Disease: DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB6 (disorder) 		3 0 2 0.11 0 0
CUI: C0030105
Disease: Ozena (disorder)
Ozena (disorder) 		4 0 2 1.0E-01 0 0
CUI: C0236053
Disease: Mucosal ulcer
Mucosal ulcer 		15 0 3 1.0E-01 0 0
CUI: C0265336
Disease: Senter syndrome
Senter syndrome 		4 30 2 1.0E-01 1 2.6E-02
CUI: C1844678
Disease: Progressive hearing loss stapes fixation
Progressive hearing loss stapes fixation 		4 35 2 1.0E-01 1 2.3E-02
CUI: C1861326
Disease: Stapes ankylosis
Stapes ankylosis 		4 0 2 1.0E-01 0 0
CUI: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) 		4 98 2 1.0E-01 1 9.3E-03