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: C0271990
Disease: delta-Thalassemia
delta-Thalassemia
7 0 4 7.4E-02 0 0
CUI: C0221018
Disease: Hereditary sideroblastic anemia
Hereditary sideroblastic anemia
9 0 4 7.1E-02 0 0
Non-transfusion dependent thalassaemia
9 0 4 7.1E-02 0 0
CUI: C0581384
Disease: Chronic anemia
Chronic anemia
10 0 4 7.0E-02 0 0
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
10 0 4 7.0E-02 0 0
Hyperferritinemia, hereditary, with congenital cataracts
10 0 4 7.0E-02 0 0
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism
26 0 5 6.9E-02 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia
26 0 5 6.9E-02 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
154 0 13 6.8E-02 0 0
Familial primary pulmonary hypertension
30 0 5 6.6E-02 0 0
2-oxo-hept-3-ene-1,7-dioate hydratase activity
14 0 4 6.6E-02 0 0
CUI: C0025222
Disease: Melena
Melena
15 0 4 6.5E-02 0 0
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia
15 0 4 6.5E-02 0 0
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia
198 103 15 6.4E-02 1 7.2E-03
CUI: C0032461
Disease: Polycythemia
Polycythemia
82 0 8 6.4E-02 0 0
CUI: C0010520
Disease: Cyanosis
Cyanosis
54 0 6 6.1E-02 0 0
CUI: C0030232
Disease: Pallor
Pallor
124 0 10 6.1E-02 0 0
CUI: C0472761
Disease: Homozygous alpha thalassemia
Homozygous alpha thalassemia
19 0 4 6.1E-02 0 0
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
19 0 4 6.1E-02 0 0
CUI: C0018932
Disease: Hematochezia
Hematochezia
37 0 5 6.0E-02 0 0
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation
73 0 7 6.0E-02 0 0
CUI: C0154835
Disease: Retinal telangiectasia
Retinal telangiectasia
20 0 4 6.0E-02 0 0
CUI: C0239105
Disease: Conjunctival telangiectasis
Conjunctival telangiectasis
20 0 4 6.0E-02 0 0
CUI: C0263454
Disease: Chloracne
Chloracne
38 0 5 6.0E-02 0 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
93 0 8 5.9E-02 0 0