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: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 5.3E-02 0 0
CUI: C0235198
Disease: Unable to concentrate
Unable to concentrate 		1 1 1 5.3E-02 1 0.14
CUI: C0241424
Disease: Tongue biting
Tongue biting 		1 0 1 5.3E-02 0 0
CUI: C0268375
Disease: Autosomal dominant epidermolysis bullosa simplex
Autosomal dominant epidermolysis bullosa simplex 		1 0 1 5.3E-02 0 0
CUI: C0343111
Disease: Naegeli syndrome
Naegeli syndrome 		1 0 1 5.3E-02 0 0
CUI: C0406344
Disease: Follicular ichthyosis
Follicular ichthyosis 		1 0 1 5.3E-02 0 0
CUI: C0574763
Disease: Hair absent (finding)
Hair absent (finding) 		1 0 1 5.3E-02 0 0
CUI: C1318562
Disease: Infantile digital fibromatosis
Infantile digital fibromatosis 		1 0 1 5.3E-02 0 0
CUI: C1844615
Disease: Skin peeling/scaling (newborn)
Skin peeling/scaling (newborn) 		1 0 1 5.3E-02 0 0
CUI: C1844617
Disease: Hypoplastic-absent sebaceous glands
Hypoplastic-absent sebaceous glands 		1 0 1 5.3E-02 0 0
CUI: C1845576
Disease: Unilateral chest hypoplasia
Unilateral chest hypoplasia 		1 0 1 5.3E-02 0 0
CUI: C1848795
Disease: GRAVES DISEASE, SUSCEPTIBILITY TO, 1
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 		1 1 1 5.3E-02 1 0.14
CUI: C1852148
Disease: Reticulate pigmentation of oral mucosa
Reticulate pigmentation of oral mucosa 		1 0 1 5.3E-02 0 0
CUI: C1857692
Disease: Venous varicosities of celiac and mesenteric vessels
Venous varicosities of celiac and mesenteric vessels 		1 0 1 5.3E-02 0 0
CUI: C1862871
Disease: ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS
ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS 		1 0 1 5.3E-02 0 0
CUI: C1970757
Disease: Tooth Agenesis, Selective, X-Linked, 1
Tooth Agenesis, Selective, X-Linked, 1 		1 0 1 5.3E-02 0 0
CUI: C2675460
Disease: HAIR MORPHOLOGY 1
HAIR MORPHOLOGY 1 		1 0 1 5.3E-02 0 0
CUI: C2677481
Disease: Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant 		1 0 1 5.3E-02 0 0
CUI: C2699508
Disease: Splenic diffuse red pulp small B-cell lymphoma
Splenic diffuse red pulp small B-cell lymphoma 		1 0 1 5.3E-02 0 0
CUI: C2748531
Disease: Perifollicular fibrosis
Perifollicular fibrosis 		1 0 1 5.3E-02 0 0
CUI: C2931428
Disease: Hypodontia, X-linked
Hypodontia, X-linked 		1 0 1 5.3E-02 0 0
CUI: C3150413
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 		1 7 1 5.3E-02 1 7.7E-02
CUI: C3502469
Disease: Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia 		1 0 1 5.3E-02 0 0
CUI: C3551587
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		1 0 1 5.3E-02 0 0
CUI: C3806745
Disease: PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED 		1 0 1 5.3E-02 0 0