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: C0268130
Disease: Hereditary orotic aciduria, type 1
Hereditary orotic aciduria, type 1 		3 0 2 0.17 0 0
CUI: C1839541
Disease: Episodic ammonia intoxication
Episodic ammonia intoxication 		4 0 2 0.15 0 0
CUI: C1839531
Disease: Protein avoidance
Protein avoidance 		5 0 2 0.14 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 2 0.13 0 0
CUI: C0041471
Disease: TYPHUS
TYPHUS 		8 0 2 0.12 0 0
CUI: C0343758
Disease: Typhus group rickettsial disease
Typhus group rickettsial disease 		8 0 2 0.12 0 0
CUI: C0032310
Disease: Pneumonia, Viral
Pneumonia, Viral 		13 0 2 9.1E-02 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 9.1E-02 0 0
CUI: C0341446
Disease: Hepatic sclerosis
Hepatic sclerosis 		1 0 1 9.1E-02 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 9.1E-02 0 0
CUI: C0948281
Disease: Malignant syndrome NOS
Malignant syndrome NOS 		1 0 1 9.1E-02 0 0
CUI: C1336139
Disease: Stage IB Non-Small Cell Lung Carcinoma AJCC v7
Stage IB Non-Small Cell Lung Carcinoma AJCC v7 		1 0 1 9.1E-02 0 0
CUI: C1836723
Disease: Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum 		1 0 1 9.1E-02 0 0
CUI: C1853800
Disease: Familial Wilms tumor 2
Familial Wilms tumor 2 		1 0 1 9.1E-02 0 0
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		1 0 1 9.1E-02 0 0
CUI: C2676507
Disease: Inflammatory Bowel Disease 21
Inflammatory Bowel Disease 21 		1 0 1 9.1E-02 0 0
CUI: C2931899
Disease: Papillary renal cell carcinoma, familial
Papillary renal cell carcinoma, familial 		1 0 1 9.1E-02 0 0
CUI: C3714958
Disease: PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO
PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 9.1E-02 0 0
CUI: C3826590
Disease: Chest--Tumors
Chest--Tumors 		1 0 1 9.1E-02 0 0
CUI: C3888880
Disease: Rhonchopathy
Rhonchopathy 		1 0 1 9.1E-02 0 0
CUI: C4017428
Disease: CERULOPLASMIN BELFAST PHENOTYPE
CERULOPLASMIN BELFAST PHENOTYPE 		1 0 1 9.1E-02 0 0
CUI: C4023070
Disease: Abnormality of ornithine metabolism
Abnormality of ornithine metabolism 		1 0 1 9.1E-02 0 0
CUI: C4084709
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97
DEAFNESS, AUTOSOMAL RECESSIVE 97 		1 0 1 9.1E-02 0 0
CUI: C4724264
Disease: stage IB non-small cell lung cancer
stage IB non-small cell lung cancer 		1 0 1 9.1E-02 0 0
CUI: C4744722
Disease: Advanced Cervical Carcinoma
Advanced Cervical Carcinoma 		1 0 1 9.1E-02 0 0