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: C0038355
Disease: Stomach Diverticulum
Stomach Diverticulum 		1 0 1 6.7E-02 0 0
CUI: C0240709
Disease: Pericardial constriction
Pericardial constriction 		1 0 1 6.7E-02 0 0
CUI: C0266941
Disease: Derangement of temporomandibular joint
Derangement of temporomandibular joint 		1 0 1 6.7E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 6.7E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 6.7E-02 0 0
CUI: C0277526
Disease: Dysenteric diarrhea
Dysenteric diarrhea 		1 0 1 6.7E-02 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 6.7E-02 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 6.7E-02 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 6.7E-02 0 0
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder 		1 0 1 6.7E-02 0 0
CUI: C1268937
Disease: Diarrhea-negative hemolytic uremic syndrome
Diarrhea-negative hemolytic uremic syndrome 		1 0 1 6.7E-02 0 0
CUI: C1304408
Disease: Urticarial vasculitis
Urticarial vasculitis 		1 0 1 6.7E-02 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria 		1 0 1 6.7E-02 0 0
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis 		1 0 1 6.7E-02 0 0
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C1859995
Disease: Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency 		1 0 1 6.7E-02 0 0
CUI: C1859998
Disease: CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING
CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING 		1 0 1 6.7E-02 0 0
CUI: C1969220
Disease: Depletion of components of the alternative complement pathway
Depletion of components of the alternative complement pathway 		1 0 1 6.7E-02 0 0
CUI: C2675730
Disease: Deafness, Congenital, and Onychodystrophy, Autosomal Dominant
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant 		1 0 1 6.7E-02 0 0
CUI: C2698027
Disease: Matrix Metalloproteinase 8 Measurement
Matrix Metalloproteinase 8 Measurement 		1 2 1 6.7E-02 1 5.9E-02
CUI: C2931895
Disease: Pericardial constriction with growth failure
Pericardial constriction with growth failure 		1 0 1 6.7E-02 0 0
CUI: C3151153
Disease: ADENOMA, CORTISOL-PRODUCING
ADENOMA, CORTISOL-PRODUCING 		1 0 1 6.7E-02 0 0
CUI: C3838669
Disease: Simple Virilizing 21-Hydroxylase Deficiency
Simple Virilizing 21-Hydroxylase Deficiency 		1 0 1 6.7E-02 0 0
CUI: C4025216
Disease: Prominent nasal septum
Prominent nasal septum 		1 0 1 6.7E-02 0 0
CUI: C4225321
Disease: ZIMMERMANN-LABAND SYNDROME 2
ZIMMERMANN-LABAND SYNDROME 2 		1 0 1 6.7E-02 0 0