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: C0162637
Disease: Strongylida Infections
Strongylida Infections
1 0 1 1.0E-01 0 0
CUI: C0231618
Disease: Corkscrewing
Corkscrewing
1 0 1 1.0E-01 0 0
CUI: C0238408
Disease: Hematoma of rectus sheath
Hematoma of rectus sheath
1 0 1 1.0E-01 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria
1 0 1 1.0E-01 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord
1 0 1 1.0E-01 0 0
CUI: C0272272
Disease: Systemic fibrinogenolysis
Systemic fibrinogenolysis
1 0 1 1.0E-01 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery
1 0 1 1.0E-01 0 0
Hereditary cerebrovascular amyloidosis
1 0 1 1.0E-01 0 0
CUI: C0392178
Disease: Lipiduria
Lipiduria
1 0 1 1.0E-01 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure
12 0 2 1.0E-01 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type
1 0 1 1.0E-01 0 0
CUI: C0438921
Disease: Back Pain without Radiation
Back Pain without Radiation
1 0 1 1.0E-01 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system
1 0 1 1.0E-01 0 0
CUI: C0740363
Disease: Back Pain with Radiation
Back Pain with Radiation
1 0 1 1.0E-01 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis
1 0 1 1.0E-01 0 0
CUI: C0749098
Disease: Hematoma, Subdural, Acute
Hematoma, Subdural, Acute
1 0 1 1.0E-01 0 0
CUI: C0750949
Disease: Vertebrogenic Pain Syndrome
Vertebrogenic Pain Syndrome
1 0 1 1.0E-01 0 0
CUI: C0751797
Disease: Intracranial Hematoma, Traumatic
Intracranial Hematoma, Traumatic
1 0 1 1.0E-01 0 0
CUI: C0877172
Disease: Hematoma, Epidural, Spinal
Hematoma, Epidural, Spinal
1 0 1 1.0E-01 0 0
CUI: C1390214
Disease: Internal hemorrhage
Internal hemorrhage
1 0 1 1.0E-01 0 0
CUI: C1704212
Disease: Embolus
Embolus
1 0 1 1.0E-01 0 0
CUI: C1706559
Disease: Cornea verticillata
Cornea verticillata
1 0 1 1.0E-01 0 0
Hypermobility of distal interphalangeal joints
1 0 1 1.0E-01 0 0
AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
1 0 1 1.0E-01 0 0
Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator
1 0 1 1.0E-01 0 0