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: C2316159
Disease: Oral allergy syndrome
Oral allergy syndrome 		3 0 2 0.22 0 0
CUI: C2825741
Disease: Indeterminate dendritic cell tumor
Indeterminate dendritic cell tumor 		7 0 2 0.15 0 0
CUI: C0162627
Disease: Skin Diseases, Bacterial
Skin Diseases, Bacterial 		1 0 1 0.12 0 0
CUI: C0162817
Disease: Skin Diseases, Eczematous
Skin Diseases, Eczematous 		1 0 1 0.12 0 0
CUI: C0263224
Disease: Flexural atopic dermatitis
Flexural atopic dermatitis 		1 0 1 0.12 0 0
CUI: C0267166
Disease: Gastroduodenitis
Gastroduodenitis 		1 0 1 0.12 0 0
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		1 0 1 0.12 0 0
CUI: C0344183
Disease: Exercise anaphylaxis
Exercise anaphylaxis 		1 0 1 0.12 0 0
CUI: C0431766
Disease: Congenital malformation syndromes involving limbs
Congenital malformation syndromes involving limbs 		1 0 1 0.12 0 0
CUI: C0432300
Disease: Autosomal dominant ichthyosis vulgaris
Autosomal dominant ichthyosis vulgaris 		1 0 1 0.12 0 0
CUI: C0474892
Disease: Inherited disorder of keratinization
Inherited disorder of keratinization 		1 0 1 0.12 0 0
CUI: C0740476
Disease: Biliary carcinoma
Biliary carcinoma 		1 0 1 0.12 0 0
CUI: C1276070
Disease: Infantile atopic dermatitis
Infantile atopic dermatitis 		1 0 1 0.12 0 0
CUI: C1304136
Disease: Onset of psoriasis in childhood (1-10 years)
Onset of psoriasis in childhood (1-10 years) 		1 0 1 0.12 0 0
CUI: C1304345
Disease: Occupational irritant contact dermatitis
Occupational irritant contact dermatitis 		1 0 1 0.12 0 0
CUI: C1406717
Disease: Sirenomelia syndrome
Sirenomelia syndrome 		1 0 1 0.12 0 0
CUI: C1852510
Disease: Craniofacial deafness hand syndrome
Craniofacial deafness hand syndrome 		1 0 1 0.12 0 0
CUI: C1859368
Disease: Camptodactyly of 2nd-5th fingers
Camptodactyly of 2nd-5th fingers 		1 0 1 0.12 0 0
CUI: C2675590
Disease: True anophthalmia
True anophthalmia 		1 1 1 0.12 1 1.0E-01
CUI: C2677500
Disease: Oculoauricular Syndrome
Oculoauricular Syndrome 		1 0 1 0.12 0 0
CUI: C3150657
Disease: BIRBECK GRANULE DEFICIENCY
BIRBECK GRANULE DEFICIENCY 		1 0 1 0.12 0 0
CUI: C4225301
Disease: OSTEOGENESIS IMPERFECTA, TYPE XVII
OSTEOGENESIS IMPERFECTA, TYPE XVII 		1 0 1 0.12 0 0
CUI: C4707581
Disease: Molluscum contagiosum skin infection
Molluscum contagiosum skin infection 		1 0 1 0.12 0 0
CUI: C0034188
Disease: Pyelonephritis, Xanthogranulomatous
Pyelonephritis, Xanthogranulomatous 		2 0 1 0.11 0 0
CUI: C0155096
Disease: Corneal ghost vessels
Corneal ghost vessels 		2 0 1 0.11 0 0