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: C0014127
Disease: Endocervicitis
Endocervicitis 		1 0 1 0.25 0 0
CUI: C0280297
Disease: lip and oral cavity squamous cell carcinoma
lip and oral cavity squamous cell carcinoma 		1 0 1 0.25 0 0
CUI: C0341699
Disease: Granulomatous interstitial nephritis
Granulomatous interstitial nephritis 		1 0 1 0.25 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder) 		1 0 1 0.25 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder) 		1 0 1 0.25 0 0
CUI: C0473221
Disease: Cryoglobulinemic glomerulonephritis
Cryoglobulinemic glomerulonephritis 		1 0 1 0.25 0 0
CUI: C0585187
Disease: Infected ascites
Infected ascites 		1 0 1 0.25 0 0
CUI: C1262010
Disease: Post lumbar puncture syndrome
Post lumbar puncture syndrome 		1 0 1 0.25 0 0
CUI: C1535985
Disease: Staphylococcal osteomyelitis
Staphylococcal osteomyelitis 		1 0 1 0.25 0 0
CUI: C1834478
Disease: MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS 		1 0 1 0.25 0 0
CUI: C1842035
Disease: Giant Platelet Syndrome with Thrombocytopenia
Giant Platelet Syndrome with Thrombocytopenia 		1 0 1 0.25 0 0
CUI: C1861512
Disease: Cochleosaccular degeneration of the inner ear and progressive cataracts
Cochleosaccular degeneration of the inner ear and progressive cataracts 		1 0 1 0.25 0 0
CUI: C1863659
Disease: DEAFNESS, AUTOSOMAL DOMINANT 17
DEAFNESS, AUTOSOMAL DOMINANT 17 		1 0 1 0.25 0 0
CUI: C2677550
Disease: URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2 		1 0 1 0.25 0 0
CUI: C2931716
Disease: Deafness, autosomal dominant nonsyndromic sensorineural 17
Deafness, autosomal dominant nonsyndromic sensorineural 17 		1 0 1 0.25 0 0
CUI: C4021547
Disease: Neutrophil inclusion bodies
Neutrophil inclusion bodies 		1 0 1 0.25 0 0
CUI: C4022866
Disease: Abnormal platelet shape
Abnormal platelet shape 		1 0 1 0.25 0 0
CUI: C4054945
Disease: Focal Segmental Glomerulosclerosis Collapsing Variant
Focal Segmental Glomerulosclerosis Collapsing Variant 		1 0 1 0.25 0 0
CUI: C4280711
Disease: Leukocyte inclusion bodies
Leukocyte inclusion bodies 		1 0 1 0.25 0 0
CUI: C0034188
Disease: Pyelonephritis, Xanthogranulomatous
Pyelonephritis, Xanthogranulomatous 		2 0 1 0.20 0 0
CUI: C0264949
Disease: Burn shock
Burn shock 		2 0 1 0.20 0 0
CUI: C0268113
Disease: Familial juvenile gout
Familial juvenile gout 		2 0 1 0.20 0 0
CUI: C0277792
Disease: Pathognomonic sign
Pathognomonic sign 		2 0 1 0.20 0 0
CUI: C0342957
Disease: Postoperative septic shock
Postoperative septic shock 		2 0 1 0.20 0 0
CUI: C0577657
Disease: Infected hand
Infected hand 		2 0 1 0.20 0 0