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: C0001261
Disease: Actinomycosis
Actinomycosis 		1 0 1 5.6E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 5.6E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 5.6E-02 0 0
CUI: C0234022
Disease: Anorgasmia
Anorgasmia 		1 0 1 5.6E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 5.6E-02 0 0
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas 		1 0 1 5.6E-02 0 0
CUI: C0333295
Disease: Acute ulcer
Acute ulcer 		1 0 1 5.6E-02 0 0
CUI: C0339678
Disease: Simple myopia
Simple myopia 		1 0 1 5.6E-02 0 0
CUI: C0423693
Disease: Growing pains
Growing pains 		1 0 1 5.6E-02 0 0
CUI: C0523550
Disease: Catalase measurement
Catalase measurement 		1 0 1 5.6E-02 0 0
CUI: C0746604
Disease: Mitral valve endocarditis
Mitral valve endocarditis 		1 0 1 5.6E-02 0 0
CUI: C0748534
Disease: sciatic nerve inflammation
sciatic nerve inflammation 		1 0 1 5.6E-02 0 0
CUI: C0752048
Disease: Hypocatalasemia
Hypocatalasemia 		1 0 1 5.6E-02 0 0
CUI: C1096352
Disease: Pancreatic enlargement
Pancreatic enlargement 		1 0 1 5.6E-02 0 0
CUI: C1171363
Disease: Renoprival hypertension
Renoprival hypertension 		1 0 1 5.6E-02 0 0
CUI: C1536651
Disease: Arterial leg ulcer
Arterial leg ulcer 		1 0 1 5.6E-02 0 0
CUI: C1843983
Disease: Trapezoidal distal femoral condyles
Trapezoidal distal femoral condyles 		1 0 1 5.6E-02 0 0
CUI: C1843985
Disease: Shortening of the talar neck
Shortening of the talar neck 		1 0 1 5.6E-02 0 0
CUI: C1843986
Disease: Flattening of the talar dome
Flattening of the talar dome 		1 0 1 5.6E-02 0 0
CUI: C1859135
Disease: Calcific stippling of infantile cartilaginous skeleton
Calcific stippling of infantile cartilaginous skeleton 		1 0 1 5.6E-02 0 0
CUI: C1859231
Disease: Hypoplastic olfactory lobes
Hypoplastic olfactory lobes 		1 0 1 5.6E-02 0 0
CUI: C1866340
Disease: Peroxisome Biogenesis Disorder, Complementation Group 3
Peroxisome Biogenesis Disorder, Complementation Group 3 		1 0 1 5.6E-02 0 0
CUI: C1866351
Disease: Peroxisome Biogenesis Disorder, Complementation Group 11
Peroxisome Biogenesis Disorder, Complementation Group 11 		1 0 1 5.6E-02 0 0
CUI: C1866352
Disease: Peroxisome Biogenesis Disorder, Complementation Group R
Peroxisome Biogenesis Disorder, Complementation Group R 		1 0 1 5.6E-02 0 0
CUI: C1963823
Disease: Hyperlipasaemia
Hyperlipasaemia 		1 0 1 5.6E-02 0 0