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: C2718078
Disease: Deficiency of Uroporphyrinogen III Synthase
Deficiency of Uroporphyrinogen III Synthase 		0 2 0 0 1 0.25
CUI: C0022904
Disease: Lacrimal Apparatus Diseases
Lacrimal Apparatus Diseases 		1 0 1 4.0E-02 0 0
CUI: C0036219
Disease: Sarcoma, Jensen
Sarcoma, Jensen 		1 0 1 4.0E-02 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 4.0E-02 0 0
CUI: C0154089
Disease: Carcinoma in situ of penis
Carcinoma in situ of penis 		1 0 1 4.0E-02 0 0
CUI: C0154298
Disease: Acute posthaemorrhagic anaemia
Acute posthaemorrhagic anaemia 		1 0 1 4.0E-02 0 0
CUI: C0271902
Disease: Microcytic normochromic anemia
Microcytic normochromic anemia 		1 0 1 4.0E-02 0 0
CUI: C0271932
Disease: Anemia of chronic renal failure
Anemia of chronic renal failure 		1 0 1 4.0E-02 0 0
CUI: C0272080
Disease: Hemoglobin D disease
Hemoglobin D disease 		1 0 1 4.0E-02 0 0
CUI: C0278799
Disease: Endometrial cancer stage II
Endometrial cancer stage II 		1 0 1 4.0E-02 0 0
CUI: C0279822
Disease: recurrent pheochromocytoma
recurrent pheochromocytoma 		1 0 1 4.0E-02 0 0
CUI: C0472713
Disease: Anemia of renal disease
Anemia of renal disease 		1 0 1 4.0E-02 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 4.0E-02 0 0
CUI: C0543645
Disease: Heterozygous hemoglobinopathy
Heterozygous hemoglobinopathy 		1 0 1 4.0E-02 0 0
CUI: C0578736
Disease: Inguinal lymphadenopathy
Inguinal lymphadenopathy 		1 0 1 4.0E-02 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 4.0E-02 0 0
CUI: C0948437
Disease: Bone marrow dysplasia
Bone marrow dysplasia 		1 0 1 4.0E-02 0 0
CUI: C0948824
Disease: Anemia due to blood loss
Anemia due to blood loss 		1 0 1 4.0E-02 0 0
CUI: C1168215
Disease: Uremic anemia
Uremic anemia 		1 0 1 4.0E-02 0 0
CUI: C1260334
Disease: Erythropoietin-resistant anemia
Erythropoietin-resistant anemia 		1 0 1 4.0E-02 0 0
CUI: C1264000
Disease: Sickle cell-Hemoglobin O Arab disease
Sickle cell-Hemoglobin O Arab disease 		1 0 1 4.0E-02 0 0
CUI: C1264016
Disease: Familial polycythemia vera
Familial polycythemia vera 		1 0 1 4.0E-02 0 0
CUI: C1285373
Disease: Neonatal respiratory system disorder
Neonatal respiratory system disorder 		1 0 1 4.0E-02 0 0
CUI: C1291373
Disease: Deficiency of sedoheptulokinase
Deficiency of sedoheptulokinase 		1 0 1 4.0E-02 0 0
CUI: C1292231
Disease: In(Lu) phenotype (finding)
In(Lu) phenotype (finding) 		1 0 1 4.0E-02 0 0