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: C0341699
Disease: Granulomatous interstitial nephritis
Granulomatous interstitial nephritis 		1 0 1 8.3E-02 0 0
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		1 0 1 8.3E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 8.3E-02 0 0
CUI: C0473221
Disease: Cryoglobulinemic glomerulonephritis
Cryoglobulinemic glomerulonephritis 		1 0 1 8.3E-02 0 0
CUI: C0581375
Disease: Double coronary vessel disease
Double coronary vessel disease 		1 0 1 8.3E-02 0 0
CUI: C0585187
Disease: Infected ascites
Infected ascites 		1 0 1 8.3E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 8.3E-02 0 0
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		1 0 1 8.3E-02 0 0
CUI: C0857256
Disease: Unwell
Unwell 		1 0 1 8.3E-02 0 0
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		1 0 1 8.3E-02 0 0
CUI: C0948384
Disease: Cerebral hygroma
Cerebral hygroma 		1 0 1 8.3E-02 0 0
CUI: C1392046
Disease: Cardiovascular insufficiency
Cardiovascular insufficiency 		1 0 1 8.3E-02 0 0
CUI: C1516419
Disease: Cervical Mesonephric Adenocarcinoma
Cervical Mesonephric Adenocarcinoma 		1 0 1 8.3E-02 0 0
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
Estrogen Receptor Status - Clinical Trial Eligibility Criteria 		1 0 1 8.3E-02 0 0
CUI: C1517658
Disease: Cervical Keratinizing Squamous Cell Carcinoma
Cervical Keratinizing Squamous Cell Carcinoma 		1 0 1 8.3E-02 0 0
CUI: C1535985
Disease: Staphylococcal osteomyelitis
Staphylococcal osteomyelitis 		1 0 1 8.3E-02 0 0
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		1 0 1 8.3E-02 0 0
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding 		1 0 1 8.3E-02 0 0
CUI: C1852407
Disease: Prominent scrotal raphe
Prominent scrotal raphe 		1 0 1 8.3E-02 0 0
CUI: C1852411
Disease: Preauricular skin furrow
Preauricular skin furrow 		1 0 1 8.3E-02 0 0
CUI: C1852510
Disease: Craniofacial deafness hand syndrome
Craniofacial deafness hand syndrome 		1 0 1 8.3E-02 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 8.3E-02 0 0
CUI: C1863392
Disease: Abnormal morphology of the limbic system
Abnormal morphology of the limbic system 		1 0 1 8.3E-02 0 0
CUI: C1863395
Disease: Acrobrachycephaly
Acrobrachycephaly 		1 0 1 8.3E-02 0 0
CUI: C1863403
Disease: Broad distal hallux
Broad distal hallux 		1 0 1 8.3E-02 0 0