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: C0162533
Disease: Porphyrias, Hepatic
Porphyrias, Hepatic 		7 0 7 0.27 0 0
CUI: C0162568
Disease: Erythropoietic Protoporphyria
Erythropoietic Protoporphyria 		24 0 8 0.19 0 0
CUI: C0162530
Disease: Porphyria, Erythropoietic
Porphyria, Erythropoietic 		20 26 7 0.18 1 3.1E-02
CUI: C0162532
Disease: Variegate Porphyria
Variegate Porphyria 		21 24 7 0.17 2 6.9E-02
CUI: C0268328
Disease: Porphobilinogen synthase deficiency
Porphobilinogen synthase deficiency 		6 0 4 0.14 0 0
CUI: C0522153
Disease: Urine Discoloration
Urine Discoloration 		10 0 4 0.12 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 39 6 0.12 3 7.0E-02
CUI: C2718078
Disease: Deficiency of Uroporphyrinogen III Synthase
Deficiency of Uroporphyrinogen III Synthase 		3 0 3 0.12 0 0
CUI: C0162531
Disease: Hereditary Coproporphyria
Hereditary Coproporphyria 		13 0 4 0.11 0 0
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria 		103 68 13 0.11 2 2.7E-02
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		6 2 3 0.10 2 0.29
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis 		6 0 3 0.10 0 0
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 1 4 1.0E-01 1 0.14
CUI: C3203671
Disease: CYP2D6 polymorphism
CYP2D6 polymorphism 		7 0 3 1.0E-01 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 3 9.7E-02 0 0
CUI: C0581384
Disease: Chronic anemia
Chronic anemia 		10 0 3 9.1E-02 0 0
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		13 0 3 8.3E-02 0 0
CUI: C0349506
Disease: Photosensitivity of skin
Photosensitivity of skin 		91 0 9 8.3E-02 0 0
CUI: C0021141
Disease: Inappropriate ADH Syndrome
Inappropriate ADH Syndrome 		14 0 3 8.1E-02 0 0
CUI: C0036214
Disease: Sarcoma, Engelbreth-Holm-Swarm
Sarcoma, Engelbreth-Holm-Swarm 		2 0 2 7.7E-02 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 2 7.7E-02 0 0
CUI: C0232488
Disease: Abdominal colic
Abdominal colic 		2 0 2 7.7E-02 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 2 7.7E-02 3 0.30
CUI: C2936779
Disease: Hydroxymethylbilane Synthase Deficiency
Hydroxymethylbilane Synthase Deficiency 		2 0 2 7.7E-02 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 2 7.7E-02 0 0