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: C4025733
Disease: Mesangial abnormality
Mesangial abnormality 		1 0 1 0.12 0 0
CUI: C4275028
Disease: Paternal uniparental disomy of chromosome 20
Paternal uniparental disomy of chromosome 20 		1 0 1 0.12 0 0
CUI: C4546184
Disease: Imprinting error
Imprinting error 		1 0 1 0.12 0 0
CUI: C4707010
Disease: Mosaic trisomy 2 syndrome
Mosaic trisomy 2 syndrome 		1 0 1 0.12 0 0
CUI: C0345907
Disease: Angiosarcoma of liver
Angiosarcoma of liver 		11 0 2 0.12 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 0 1 0.11 0 0
CUI: C0268749
Disease: Fibrillary glomerulonephritis
Fibrillary glomerulonephritis 		2 0 1 0.11 0 0
CUI: C0342957
Disease: Postoperative septic shock
Postoperative septic shock 		2 0 1 0.11 0 0
CUI: C0432221
Disease: Spondylometaphyseal dysplasia, 'corner fracture' type
Spondylometaphyseal dysplasia, 'corner fracture' type 		2 0 1 0.11 0 0
CUI: C0578438
Disease: Adenocarcinoma of sigmoid colon
Adenocarcinoma of sigmoid colon 		2 0 1 0.11 0 0
CUI: C0852519
Disease: Benign chondrogenic neoplasm
Benign chondrogenic neoplasm 		2 0 1 0.11 0 0
CUI: C2931746
Disease: Sulfocysteinuria
Sulfocysteinuria 		2 0 1 0.11 0 0
CUI: C0524702
Disease: Pulmonary Thromboembolisms
Pulmonary Thromboembolisms 		33 0 4 0.11 0 0
CUI: C0035793
Disease: Rocky Mountain Spotted Fever
Rocky Mountain Spotted Fever 		3 0 1 1.0E-01 0 0
CUI: C0162569
Disease: Hepatoerythropoietic Porphyria
Hepatoerythropoietic Porphyria 		3 0 1 1.0E-01 0 0
CUI: C0263560
Disease: Chronic ulcer of lower extremity
Chronic ulcer of lower extremity 		3 0 1 1.0E-01 0 0
CUI: C0398359
Disease: Trousseau's syndrome
Trousseau's syndrome 		3 0 1 1.0E-01 0 0
CUI: C1288350
Disease: Subretinal membrane
Subretinal membrane 		3 0 1 1.0E-01 0 0
CUI: C1610605
Disease: Graft versus host disease in skin
Graft versus host disease in skin 		3 0 1 1.0E-01 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		3 0 1 1.0E-01 0 0
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 1 1.0E-01 0 0
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		26 0 3 9.7E-02 0 0
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		26 0 3 9.7E-02 0 0
CUI: C0009492
Disease: Compartment syndromes
Compartment syndromes 		4 0 1 9.1E-02 0 0
CUI: C0032308
Disease: Staphylococcal Pneumonia
Staphylococcal Pneumonia 		4 0 1 9.1E-02 0 0