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: C0041971
Disease: Urethral Neoplasms
Urethral Neoplasms 		1 0 1 4.5E-02 0 0
CUI: C0152454
Disease: Symblepharon
Symblepharon 		1 0 1 4.5E-02 0 0
CUI: C0241424
Disease: Tongue biting
Tongue biting 		1 0 1 4.5E-02 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 4.5E-02 0 0
CUI: C0265971
Disease: Acrokeratosis Verruciformis of Hopf
Acrokeratosis Verruciformis of Hopf 		1 0 1 4.5E-02 0 0
CUI: C0268375
Disease: Autosomal dominant epidermolysis bullosa simplex
Autosomal dominant epidermolysis bullosa simplex 		1 0 1 4.5E-02 0 0
CUI: C0343111
Disease: Naegeli syndrome
Naegeli syndrome 		1 0 1 4.5E-02 0 0
CUI: C0406716
Disease: Hypodontia and nail dysgenesis
Hypodontia and nail dysgenesis 		1 0 1 4.5E-02 0 0
CUI: C0432267
Disease: Tricho-thiodystrophy disorder
Tricho-thiodystrophy disorder 		1 0 1 4.5E-02 0 0
CUI: C0473575
Disease: Acantholytic Dyskeratotic Epidermal Nevus
Acantholytic Dyskeratotic Epidermal Nevus 		1 0 1 4.5E-02 0 0
CUI: C0477325
Disease: Immunodeficiency associated with other specified major defects
Immunodeficiency associated with other specified major defects 		1 0 1 4.5E-02 0 0
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		1 0 1 4.5E-02 0 0
CUI: C0858699
Disease: Skin keratosis
Skin keratosis 		1 0 1 4.5E-02 0 0
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		1 0 1 4.5E-02 0 0
CUI: C1313961
Disease: Trichorrhexis nodosa syndrome
Trichorrhexis nodosa syndrome 		1 0 1 4.5E-02 0 0
CUI: C1318562
Disease: Infantile digital fibromatosis
Infantile digital fibromatosis 		1 0 1 4.5E-02 0 0
CUI: C1327916
Disease: REVESZ SYNDROME (disorder)
REVESZ SYNDROME (disorder) 		1 0 1 4.5E-02 0 0
CUI: C1704335
Disease: Apocrine cystadenoma
Apocrine cystadenoma 		1 0 1 4.5E-02 0 0
CUI: C1834383
Disease: Thickening of the lateral border of the scapula
Thickening of the lateral border of the scapula 		1 0 1 4.5E-02 0 0
CUI: C1834392
Disease: Disproportionate prominence of the femoral medial condyle
Disproportionate prominence of the femoral medial condyle 		1 0 1 4.5E-02 0 0
CUI: C1835492
Disease: TOOTH AGENESIS, SELECTIVE, 4 (disorder)
TOOTH AGENESIS, SELECTIVE, 4 (disorder) 		1 0 1 4.5E-02 0 0
CUI: C1835493
Disease: Succedaneous Teeth, Agenesis Of
Succedaneous Teeth, Agenesis Of 		1 0 1 4.5E-02 0 0
CUI: C1844722
Disease: Unilateral breast hypoplasia
Unilateral breast hypoplasia 		1 0 1 4.5E-02 0 0
CUI: C1845073
Disease: INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 (disorder)
INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 (disorder) 		1 0 1 4.5E-02 0 0
CUI: C1845919
Disease: Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema 		1 0 1 4.5E-02 0 0