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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		22 11 7 0.23 5 0.17
CUI: C0221018
Disease: Hereditary sideroblastic anemia
Hereditary sideroblastic anemia 		9 1 4 0.19 1 4.3E-02
CUI: C0750992
Disease: Catatonia, Malignant
Catatonia, Malignant 		5 0 3 0.17 0 0
CUI: C0268225
Disease: Aspartylglucosaminuria
Aspartylglucosaminuria 		9 0 3 0.14 0 0
CUI: C0349653
Disease: Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1A 		10 0 3 0.13 0 0
CUI: C2673914
Disease: Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 		2 0 2 0.12 0 0
CUI: C4225425
Disease: ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY
ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY 		2 0 2 0.12 0 0
CUI: C0920372
Disease: Carcinogenesis, Radiation
Carcinogenesis, Radiation 		13 0 3 0.12 0 0
CUI: C1862839
Disease: Anterior segment mesenchymal dysgenesis
Anterior segment mesenchymal dysgenesis 		13 0 3 0.12 0 0
CUI: C1835993
Disease: Loss of ability to walk in early childhood
Loss of ability to walk in early childhood 		4 0 2 0.11 0 0
CUI: C1263988
Disease: Hemolytic disorder
Hemolytic disorder 		15 0 3 0.11 0 0
CUI: C0333912
Disease: Hypochromatism
Hypochromatism 		5 0 2 0.11 0 0
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		5 4 2 0.11 1 3.8E-02
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		16 0 3 0.10 0 0
CUI: C0234935
Disease: Acute urticaria
Acute urticaria 		17 0 3 1.0E-01 0 0
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		6 2 2 1.0E-01 1 4.2E-02
CUI: C0855790
Disease: Decreased mean corpuscular volume
Decreased mean corpuscular volume 		6 0 2 1.0E-01 0 0
CUI: C3666003
Disease: Transfusion dependent anaemia
Transfusion dependent anaemia 		6 0 2 1.0E-01 0 0
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		19 0 3 9.4E-02 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 2 9.1E-02 0 0
CUI: C0025237
Disease: Melnick-Needles Syndrome
Melnick-Needles Syndrome 		23 0 3 8.3E-02 0 0
CUI: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		23 0 3 8.3E-02 0 0
CUI: C0581384
Disease: Chronic anemia
Chronic anemia 		10 0 2 8.3E-02 0 0
CUI: C1264195
Disease: Refractory anemia with ringed sideroblasts
Refractory anemia with ringed sideroblasts 		36 3 4 8.3E-02 1 4.0E-02
CUI: C1704380
Disease: Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis 		23 0 3 8.3E-02 0 0