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 5 0.22 0 0
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism 		26 7 7 0.17 2 6.9E-02
CUI: C0162568
Disease: Erythropoietic Protoporphyria
Erythropoietic Protoporphyria 		24 0 5 0.12 0 0
CUI: C0268328
Disease: Porphobilinogen synthase deficiency
Porphobilinogen synthase deficiency 		6 0 3 0.12 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 3 0.12 0 0
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda 		30 39 5 0.11 1 1.6E-02
CUI: C0162531
Disease: Hereditary Coproporphyria
Hereditary Coproporphyria 		13 0 3 9.7E-02 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 2 9.5E-02 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 2 9.5E-02 1 3.4E-02
CUI: C2936779
Disease: Hydroxymethylbilane Synthase Deficiency
Hydroxymethylbilane Synthase Deficiency 		2 0 2 9.5E-02 0 0
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 2 9.5E-02 0 0
CUI: C0021141
Disease: Inappropriate ADH Syndrome
Inappropriate ADH Syndrome 		14 0 3 9.4E-02 0 0
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 2 9.1E-02 0 0
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		4 3 2 8.7E-02 1 3.8E-02
CUI: C1867971
Disease: Acute episodes of neuropathic symptoms
Acute episodes of neuropathic symptoms 		4 0 2 8.7E-02 0 0
CUI: C0751753
Disease: Carbamoyl-Phosphate Synthase I Deficiency Disease
Carbamoyl-Phosphate Synthase I Deficiency Disease 		18 0 3 8.3E-02 0 0
CUI: C0027583
Disease: Nematode infections
Nematode infections 		33 0 4 8.0E-02 0 0
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		6 2 2 8.0E-02 1 4.0E-02
CUI: C0162530
Disease: Porphyria, Erythropoietic
Porphyria, Erythropoietic 		20 0 3 7.9E-02 0 0
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria 		103 0 9 7.8E-02 0 0
CUI: C1851400
Disease: Facial Hypertrichosis
Facial Hypertrichosis 		8 0 2 7.4E-02 0 0
CUI: C3553943
Disease: T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS 		8 0 2 7.4E-02 0 0
CUI: C0522153
Disease: Urine Discoloration
Urine Discoloration 		10 0 2 6.9E-02 0 0
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		13 0 2 6.2E-02 0 0
CUI: C0267792
Disease: Hepatobiliary disease
Hepatobiliary disease 		14 0 2 6.1E-02 0 0