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: C0277941
Disease: Blanching of skin
Blanching of skin 		1 0 1 2.0E-02 0 0
CUI: C0277977
Disease: Murphy's sign
Murphy's sign 		1 0 1 2.0E-02 0 0
CUI: C0333295
Disease: Acute ulcer
Acute ulcer 		1 0 1 2.0E-02 0 0
CUI: C0333814
Disease: Pappenheimer body (morphologic abnormality)
Pappenheimer body (morphologic abnormality) 		1 0 1 2.0E-02 0 0
CUI: C0396009
Disease: Pharyngocutaneous fistula
Pharyngocutaneous fistula 		1 0 1 2.0E-02 0 0
CUI: C0401013
Disease: Fungal peritonitis
Fungal peritonitis 		1 0 1 2.0E-02 0 0
CUI: C0410648
Disease: Spinal instability
Spinal instability 		1 0 1 2.0E-02 0 0
CUI: C0472713
Disease: Anemia of renal disease
Anemia of renal disease 		1 0 1 2.0E-02 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 2.0E-02 0 0
CUI: C0476337
Disease: Blood gases abnormal
Blood gases abnormal 		1 0 1 2.0E-02 0 0
CUI: C0523550
Disease: Catalase measurement
Catalase measurement 		1 0 1 2.0E-02 0 0
CUI: C0543645
Disease: Heterozygous hemoglobinopathy
Heterozygous hemoglobinopathy 		1 0 1 2.0E-02 0 0
CUI: C0578736
Disease: Inguinal lymphadenopathy
Inguinal lymphadenopathy 		1 0 1 2.0E-02 0 0
CUI: C0741026
Disease: Atypical angina
Atypical angina 		1 0 1 2.0E-02 0 0
CUI: C0746604
Disease: Mitral valve endocarditis
Mitral valve endocarditis 		1 0 1 2.0E-02 0 0
CUI: C0752048
Disease: Hypocatalasemia
Hypocatalasemia 		1 0 1 2.0E-02 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 2.0E-02 0 0
CUI: C0853689
Disease: Secondary hyperlipidemia
Secondary hyperlipidemia 		1 0 1 2.0E-02 0 0
CUI: C0860549
Disease: Refeeding Syndrome
Refeeding Syndrome 		1 0 1 2.0E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 2.0E-02 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease 		1 0 1 2.0E-02 0 0
CUI: C0878666
Disease: Analbuminemia
Analbuminemia 		1 0 1 2.0E-02 0 0
CUI: C0936251
Disease: Polyradiculitis
Polyradiculitis 		1 0 1 2.0E-02 0 0
CUI: C0948437
Disease: Bone marrow dysplasia
Bone marrow dysplasia 		1 0 1 2.0E-02 0 0
CUI: C1167806
Disease: Increased alpha-globulin
Increased alpha-globulin 		1 0 1 2.0E-02 0 0