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 		0 11 0 0 1 2.4E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0 220 0 0 1 4.0E-03
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		0 3 0 0 1 3.0E-02
CUI: C0018862
Disease: Heberden node
Heberden node 		0 1 0 0 1 3.2E-02
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis 		0 2 0 0 1 3.1E-02
CUI: C0024215
Disease: Lymphangiectasis, Intestinal
Lymphangiectasis, Intestinal 		0 1 0 0 1 3.2E-02
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism 		0 7 0 0 1 2.7E-02
CUI: C0162531
Disease: Hereditary Coproporphyria
Hereditary Coproporphyria 		0 11 0 0 1 2.4E-02
CUI: C0162532
Disease: Variegate Porphyria
Variegate Porphyria 		0 24 0 0 1 1.9E-02
CUI: C0235280
Disease: Ototoxicity
Ototoxicity 		0 6 0 0 1 2.8E-02
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly 		0 8 0 0 1 2.6E-02
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		0 8 0 0 1 2.6E-02
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 3.2E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 3.2E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 2.8E-02
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		0 2 0 0 1 3.1E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 2.0E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0 344 0 0 1 2.7E-03
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis 		0 13 0 0 1 2.3E-02
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		0 3 0 0 1 3.0E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 2.0E-02
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		0 2 0 0 1 3.1E-02
CUI: C0858321
Disease: Plasmodium vivax infection
Plasmodium vivax infection 		0 1 0 0 1 3.2E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 3.1E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 3.0E-02