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: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome 		0 6 0 0 1 8.3E-02
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 4.3E-02 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 4.3E-02 0 0
CUI: C0263925
Disease: Iliac crest spur
Iliac crest spur 		1 0 1 4.3E-02 0 0
CUI: C0268796
Disease: Arteriolar nephrosclerosis
Arteriolar nephrosclerosis 		1 0 1 4.3E-02 0 0
CUI: C0272240
Disease: Disorder of complement
Disorder of complement 		1 0 1 4.3E-02 0 0
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage 		1 0 1 4.3E-02 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder) 		1 0 1 4.3E-02 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder) 		1 0 1 4.3E-02 0 0
CUI: C0431709
Disease: Adult type polycystic kidney disease type 1
Adult type polycystic kidney disease type 1 		1 0 1 4.3E-02 0 0
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement 		1 0 1 4.3E-02 0 0
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		1 0 1 4.3E-02 0 0
CUI: C0859023
Disease: Talkativeness
Talkativeness 		1 0 1 4.3E-02 0 0
CUI: C1264422
Disease: Blister with infection
Blister with infection 		1 0 1 4.3E-02 0 0
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar 		1 0 1 4.3E-02 0 0
CUI: C1834383
Disease: Thickening of the lateral border of the scapula
Thickening of the lateral border of the scapula 		1 0 1 4.3E-02 0 0
CUI: C1834392
Disease: Disproportionate prominence of the femoral medial condyle
Disproportionate prominence of the femoral medial condyle 		1 0 1 4.3E-02 0 0
CUI: C1834478
Disease: MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS 		1 0 1 4.3E-02 0 0
CUI: C1836890
Disease: Hypoplasia of the ciliary body
Hypoplasia of the ciliary body 		1 0 1 4.3E-02 0 0
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		1 0 1 4.3E-02 0 0
CUI: C1838818
Disease: MUSCLE STIFFNESS, PAINFUL
MUSCLE STIFFNESS, PAINFUL 		1 0 1 4.3E-02 0 0
CUI: C1842035
Disease: Giant Platelet Syndrome with Thrombocytopenia
Giant Platelet Syndrome with Thrombocytopenia 		1 0 1 4.3E-02 0 0
CUI: C1842982
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO 		1 0 1 4.3E-02 0 0
CUI: C1855758
Disease: Lateral displacement of the femoral head
Lateral displacement of the femoral head 		1 0 1 4.3E-02 0 0
CUI: C1858915
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2 		1 0 1 4.3E-02 0 0