Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Adult type polycystic kidney disease type 1
1 0 1 0.25 0 0
CUI: C1282310
Disease: Intermittent pain
Intermittent pain
1 0 1 0.25 0 0
CUI: C1334377
Disease: Laryngeal Sarcoma
Laryngeal Sarcoma
1 0 1 0.25 0 0
Acute Hemolytic Transfusion Reaction
1 0 1 0.25 0 0
CUI: C4022832
Disease: Mild proteinuria
Mild proteinuria
1 0 1 0.25 0 0
CUI: C4225313
Disease: BETHLEM MYOPATHY 2
BETHLEM MYOPATHY 2
1 0 1 0.25 0 0
ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2
1 0 1 0.25 0 0
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
1 0 1 0.25 0 0
CUI: C0232492
Disease: Upper abdominal pain
Upper abdominal pain
2 0 1 0.20 0 0
Prolapsed thoracic intervertebral disc
2 0 1 0.20 0 0
CUI: C0477728
Disease: Hereditary nephropathy
Hereditary nephropathy
2 0 1 0.20 0 0
CUI: C0520962
Disease: Localized pain
Localized pain
2 0 1 0.20 0 0
CUI: C0746984
Disease: Obstructive ventilatory defect
Obstructive ventilatory defect
2 0 1 0.20 0 0
CUI: C0795805
Disease: Chromosome 2, trisomy 2q
Chromosome 2, trisomy 2q
2 0 1 0.20 0 0
Leiomyomatosis, esophageal and vulval, with nephropathy
2 0 1 0.20 0 0
CUI: C1865276
Disease: Global glomerulosclerosis
Global glomerulosclerosis
2 0 1 0.20 0 0
CUI: C2585107
Disease: Asymptomatic multiple myeloma
Asymptomatic multiple myeloma
2 0 1 0.20 0 0
CUI: C2700593
Disease: Cystic dermoid choristoma
Cystic dermoid choristoma
2 0 1 0.20 0 0
MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME
2 0 1 0.20 0 0
CUI: C3900051
Disease: Amotivation
Amotivation
2 0 1 0.20 0 0
CUI: C4024984
Disease: Diffuse leiomyomatosis
Diffuse leiomyomatosis
2 0 1 0.20 0 0
CUI: C4746986
Disease: ALPORT SYNDROME 1, X-LINKED
ALPORT SYNDROME 1, X-LINKED
2 0 1 0.20 0 0
CUI: C0264192
Disease: Pelvic obliquity
Pelvic obliquity
3 0 1 0.17 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus
3 0 1 0.17 0 0
CUI: C1262148
Disease: Grip strength decreased
Grip strength decreased
3 0 1 0.17 0 0