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: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait 		34 0 4 1.0E-01 0 0
CUI: C1863224
Disease: Adenosine Triphosphate, Elevated, Of Erythrocytes
Adenosine Triphosphate, Elevated, Of Erythrocytes 		1 0 1 1.0E-01 0 0
CUI: C1865614
Disease: HEMOCHROMATOSIS, TYPE 2A
HEMOCHROMATOSIS, TYPE 2A 		1 0 1 1.0E-01 0 0
CUI: C1865616
Disease: HEMOCHROMATOSIS, TYPE 2B
HEMOCHROMATOSIS, TYPE 2B 		1 0 1 1.0E-01 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 0 1 1.0E-01 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 1.0E-01 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 1.0E-01 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 0 1 1.0E-01 0 0
CUI: C3489571
Disease: Familial Extrahepatic Biliary Atresia
Familial Extrahepatic Biliary Atresia 		1 0 1 1.0E-01 0 0
CUI: C3489572
Disease: Idiopathic Extrahepatic Biliary Atresia
Idiopathic Extrahepatic Biliary Atresia 		1 0 1 1.0E-01 0 0
CUI: C3808920
Disease: ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2 		1 0 1 1.0E-01 0 0
CUI: C4016851
Disease: BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY 		1 0 1 1.0E-01 0 0
CUI: C4023032
Disease: Dysplastic erythropoesis
Dysplastic erythropoesis 		1 0 1 1.0E-01 0 0
CUI: C4025631
Disease: Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes
Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes 		1 0 1 1.0E-01 0 0
CUI: C4025798
Disease: Abnormalities of placenta or umbilical cord
Abnormalities of placenta or umbilical cord 		1 0 1 1.0E-01 0 0
CUI: C4293689
Disease: Abnormal proerythroblast morphology
Abnormal proerythroblast morphology 		1 0 1 1.0E-01 0 0
CUI: C4304539
Disease: 20p12.3 microdeletion syndrome
20p12.3 microdeletion syndrome 		1 0 1 1.0E-01 0 0
CUI: C4476595
Disease: Reduced red cell pyruvate kinase activity
Reduced red cell pyruvate kinase activity 		1 0 1 1.0E-01 0 0
CUI: C4693481
Disease: SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES
SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 		1 0 1 1.0E-01 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea 		37 0 4 9.3E-02 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 9.1E-02 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 0 1 9.1E-02 0 0
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 9.1E-02 0 0