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: C0268371
Disease: Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails 		1 10 1 1.00 9 0.64
CUI: C0474886
Disease: Localized recessive dystrophic epidermolysis bullosa
Localized recessive dystrophic epidermolysis bullosa 		1 0 1 1.00 0 0
CUI: C0474887
Disease: Generalized dystrophic epidermolysis bullosa
Generalized dystrophic epidermolysis bullosa 		1 0 1 1.00 0 0
CUI: C1851573
Disease: Transient bullous dermolysis of the newborn
Transient bullous dermolysis of the newborn 		1 13 1 1.00 10 0.62
CUI: C1853063
Disease: EPIDERMOLYSIS BULLOSA PRURIGINOSA, AUTOSOMAL RECESSIVE
EPIDERMOLYSIS BULLOSA PRURIGINOSA, AUTOSOMAL RECESSIVE 		1 0 1 1.00 0 0
CUI: C2675780
Disease: EPIDERMOLYSIS BULLOSA PRURIGINOSA, AUTOSOMAL DOMINANT
EPIDERMOLYSIS BULLOSA PRURIGINOSA, AUTOSOMAL DOMINANT 		1 3 1 1.00 1 6.7E-02
CUI: C4015945
Disease: EPIDERMOLYSIS BULLOSA, PRETIBIAL, AUTOSOMAL RECESSIVE
EPIDERMOLYSIS BULLOSA, PRETIBIAL, AUTOSOMAL RECESSIVE 		1 0 1 1.00 0 0
CUI: C4510043
Disease: Severe generalized recessive dystrophic epidermolysis bullosa
Severe generalized recessive dystrophic epidermolysis bullosa 		1 0 1 1.00 0 0
CUI: C4511056
Disease: Centripetalis recessive dystrophic epidermolysis bullosa
Centripetalis recessive dystrophic epidermolysis bullosa 		1 0 1 1.00 0 0
CUI: C4518087
Disease: Acral dystrophic epidermolysis bullosa
Acral dystrophic epidermolysis bullosa 		1 0 1 1.00 0 0
CUI: C0079136
Disease: Cockayne-Touraine Disease
Cockayne-Touraine Disease 		2 3 1 0.50 2 0.14
CUI: C0238115
Disease: Boerhaave syndrome
Boerhaave syndrome 		2 0 1 0.50 0 0
CUI: C0432322
Disease: Dominant dystrophic epidermolysis bullosa, albopapular type (disorder)
Dominant dystrophic epidermolysis bullosa, albopapular type (disorder) 		2 25 1 0.50 11 0.41
CUI: C2931648
Disease: Larsen syndrome, dominant type
Larsen syndrome, dominant type 		2 0 1 0.50 0 0
CUI: C0432321
Disease: Epidermolysis bullosa, pretibial
Epidermolysis bullosa, pretibial 		3 10 1 0.33 9 0.64
CUI: C1275114
Disease: Epidermolysis Bullosa Pruriginosa
Epidermolysis Bullosa Pruriginosa 		3 11 1 0.33 9 0.60
CUI: C1864694
Disease: Complement Component 7 Deficiency
Complement Component 7 Deficiency 		3 0 1 0.33 0 0
CUI: C2673611
Disease: Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant
Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant 		3 0 1 0.33 0 0
CUI: C2673612
Disease: Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive
Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive 		3 4 1 0.33 1 6.2E-02
CUI: C0271321
Disease: Madarosis of eyelid
Madarosis of eyelid 		4 0 1 0.25 0 0
CUI: C3277900
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4 		4 13 1 0.25 1 4.0E-02
CUI: C4024876
Disease: Palmoplantar blistering
Palmoplantar blistering 		4 0 1 0.25 0 0
CUI: C4316878
Disease: Loss of eyelashes
Loss of eyelashes 		4 0 1 0.25 0 0
CUI: C0175778
Disease: Larsen syndrome
Larsen syndrome 		6 0 1 0.17 0 0
CUI: C2673597
Disease: Congenital localized absence of skin
Congenital localized absence of skin 		6 0 1 0.17 0 0