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: C0221245
Disease: Fissure in skin
Fissure in skin 		3 0 3 0.30 0 0
CUI: C0038605
Disease: Subungual hyperkeratosis
Subungual hyperkeratosis 		5 0 3 0.25 0 0
CUI: C2609071
Disease: Olmsted syndrome
Olmsted syndrome 		5 0 3 0.25 0 0
CUI: C1275091
Disease: Ichthyosis follicularis with alopecia and photophobia (IFAP)
Ichthyosis follicularis with alopecia and photophobia (IFAP) 		2 0 2 0.20 0 0
CUI: C3670629
Disease: Orthokeratotic hyperkeratosis
Orthokeratotic hyperkeratosis 		3 0 2 0.18 0 0
CUI: C3277900
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4 		4 0 2 0.17 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		13 0 3 0.15 0 0
CUI: C0003090
Disease: Ankylosis
Ankylosis 		15 0 3 0.14 0 0
CUI: C0016436
Disease: Folliculitis
Folliculitis 		9 0 2 0.12 0 0
CUI: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 1.0E-01 0 0
CUI: C0037753
Disease: Sparganosis
Sparganosis 		1 0 1 1.0E-01 0 0
CUI: C0277960
Disease: Dry hair
Dry hair 		12 0 2 1.0E-01 0 0
CUI: C0333525
Disease: Maceration
Maceration 		1 0 1 1.0E-01 0 0
CUI: C0406344
Disease: Follicular ichthyosis
Follicular ichthyosis 		1 0 1 1.0E-01 0 0
CUI: C0406369
Disease: Lichen planus pemphigoides
Lichen planus pemphigoides 		1 0 1 1.0E-01 0 0
CUI: C0558143
Disease: Macerated skin (finding)
Macerated skin (finding) 		1 0 1 1.0E-01 0 0
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		1 0 1 1.0E-01 0 0
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		1 0 1 1.0E-01 0 0
CUI: C1304224
Disease: Pemphigoid nodularis
Pemphigoid nodularis 		1 0 1 1.0E-01 0 0
CUI: C1336862
Disease: Parotid Gland Undifferentiated Carcinoma
Parotid Gland Undifferentiated Carcinoma 		1 0 1 1.0E-01 0 0
CUI: C1565106
Disease: Headache Disorders, Primary
Headache Disorders, Primary 		1 0 1 1.0E-01 0 0
CUI: C1704335
Disease: Apocrine cystadenoma
Apocrine cystadenoma 		1 0 1 1.0E-01 0 0
CUI: C1835492
Disease: TOOTH AGENESIS, SELECTIVE, 4 (disorder)
TOOTH AGENESIS, SELECTIVE, 4 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1835493
Disease: Succedaneous Teeth, Agenesis Of
Succedaneous Teeth, Agenesis Of 		1 0 1 1.0E-01 0 0
CUI: C1845576
Disease: Unilateral chest hypoplasia
Unilateral chest hypoplasia 		1 0 1 1.0E-01 0 0