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: C0271987
Disease: ^A^gamma delta beta^0^ thalassemia
^A^gamma delta beta^0^ thalassemia
4 0 4 0.44 0 0
CUI: C4023136
Disease: Reduced alpha/beta synthesis ratio
Reduced alpha/beta synthesis ratio
4 0 4 0.44 0 0
CUI: C0271985
Disease: Delta-Beta Thalassemia
Delta-Beta Thalassemia
12 0 6 0.40 0 0
CUI: C0271986
Disease: delta beta^0^ Thalassemia
delta beta^0^ Thalassemia
10 0 5 0.36 0 0
CUI: C0271990
Disease: delta-Thalassemia
delta-Thalassemia
7 0 4 0.33 0 0
CUI: C0271991
Disease: delta^0^ Thalassemia
delta^0^ Thalassemia
3 0 3 0.33 0 0
CUI: C0272005
Disease: Hemoglobin Bart's hydrops syndrome
Hemoglobin Bart's hydrops syndrome
3 0 3 0.33 0 0
CUI: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias
3 0 3 0.33 0 0
CUI: C2825560
Disease: S-Beta Thalassemia
S-Beta Thalassemia
3 0 3 0.33 0 0
CUI: C2873754
Disease: Severe alpha thalassemia
Severe alpha thalassemia
3 0 3 0.33 0 0
CUI: C0238159
Disease: Hemoglobin E disease
Hemoglobin E disease
8 0 4 0.31 0 0
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
8 0 4 0.31 0 0
Hemoglobin E/beta thalassemia disease
4 0 3 0.30 0 0
Alpha-Thalassemia Myelodysplasia Syndrome
4 0 3 0.30 0 0
CUI: C1527405
Disease: Erythrocytosis
Erythrocytosis
9 0 4 0.29 0 0
CUI: C2873756
Disease: Severe beta thalassemia
Severe beta thalassemia
9 0 4 0.29 0 0
CUI: C4274391
Disease: Dominant beta-thalassemia
Dominant beta-thalassemia
5 0 3 0.27 0 0
CUI: C0553699
Disease: Heinz body observation
Heinz body observation
6 0 3 0.25 0 0
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement
6 0 3 0.25 0 0
CUI: C0221019
Disease: Sickle cell-beta-thalassemia
Sickle cell-beta-thalassemia
7 0 3 0.23 0 0
CUI: C3665425
Disease: Hemoglobin M Disease
Hemoglobin M Disease
7 0 3 0.23 0 0
CUI: C0272003
Disease: alpha^+^ Thalassemia, deletion type
alpha^+^ Thalassemia, deletion type
2 0 2 0.22 0 0
CUI: C0272081
Disease: Hemoglobin D trait
Hemoglobin D trait
2 0 2 0.22 0 0
Alpha-thalassemia/mental retardation syndrome (301040) is an allelic disorder
2 0 2 0.22 0 0
CUI: C1260397
Disease: Alpha thalassemia minor
Alpha thalassemia minor
2 0 2 0.22 0 0