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: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
8 0 4 0.11 0 0
CUI: C0039730
Disease: Thalassemia
Thalassemia
136 0 16 0.10 0 0
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia
198 103 21 1.0E-01 26 0.21
CUI: C4321477
Disease: Sickle Cell-SS Disease
Sickle Cell-SS Disease
62 0 8 9.1E-02 0 0
Iron-Refractory Iron Deficiency Anemia
51 0 7 9.0E-02 0 0
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia
15 0 4 8.9E-02 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 0 6 8.8E-02 0 0
CUI: C0271991
Disease: delta^0^ Thalassemia
delta^0^ Thalassemia
3 0 3 8.8E-02 0 0
CUI: C0271995
Disease: HPFH deletion type
HPFH deletion type
3 0 3 8.8E-02 0 0
CUI: C0521800
Disease: Central cyanosis
Central cyanosis
3 0 3 8.8E-02 0 0
CUI: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias
3 19 3 8.8E-02 4 6.2E-02
CUI: C2825560
Disease: S-Beta Thalassemia
S-Beta Thalassemia
3 0 3 8.8E-02 0 0
HEMOGLOBIN H HYDROPS FETALIS SYNDROME
3 0 3 8.8E-02 0 0
CUI: C0238644
Disease: Anemia, severe
Anemia, severe
65 0 8 8.8E-02 0 0
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
4 20 3 8.6E-02 4 6.2E-02
CUI: C4023136
Disease: Reduced alpha/beta synthesis ratio
Reduced alpha/beta synthesis ratio
4 0 3 8.6E-02 0 0
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor
18 0 4 8.3E-02 0 0
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor
5 0 3 8.3E-02 0 0
CUI: C3539063
Disease: Bart's Hemoglobinopathy
Bart's Hemoglobinopathy
5 0 3 8.3E-02 0 0
CUI: C0553699
Disease: Heinz body observation
Heinz body observation
6 0 3 8.1E-02 0 0
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement
6 0 3 8.1E-02 0 0
CUI: C2745948
Disease: Hyalinosis, Systemic
Hyalinosis, Systemic
20 0 4 8.0E-02 0 0
CUI: C0221019
Disease: Sickle cell-beta-thalassemia
Sickle cell-beta-thalassemia
7 0 3 7.9E-02 0 0
CUI: C3665425
Disease: Hemoglobin M Disease
Hemoglobin M Disease
7 0 3 7.9E-02 0 0
CUI: C4025630
Disease: Abnormal bone structure
Abnormal bone structure
7 0 3 7.9E-02 0 0