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: C1865903
Disease: Long-tract signs
Long-tract signs
9 0 6 0.67 0 0
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
2 0 2 0.33 0 0
Neurofibrillary degeneration (morphologic abnormality)
21 0 6 0.29 0 0
CUI: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency
3 0 2 0.29 0 0
CUI: C0751003
Disease: Brain Aneurysm
Brain Aneurysm
4 0 2 0.25 0 0
CUI: C0018814
Disease: Heart Rupture, Post-Infarction
Heart Rupture, Post-Infarction
1 0 1 0.17 0 0
CUI: C0162637
Disease: Strongylida Infections
Strongylida Infections
1 0 1 0.17 0 0
Derangement of temporomandibular joint
1 0 1 0.17 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis
1 0 1 0.17 0 0
CUI: C0272272
Disease: Systemic fibrinogenolysis
Systemic fibrinogenolysis
1 0 1 0.17 0 0
CUI: C0277526
Disease: Dysenteric diarrhea
Dysenteric diarrhea
1 0 1 0.17 0 0
Hereditary cerebrovascular amyloidosis
1 0 1 0.17 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system
1 0 1 0.17 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis
1 0 1 0.17 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin
1 0 1 0.17 0 0
CUI: C1304408
Disease: Urticarial vasculitis
Urticarial vasculitis
1 0 1 0.17 0 0
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
1 0 1 0.17 0 0
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
1 0 1 0.17 0 0
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
1 0 1 0.17 0 0
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
1 0 1 0.17 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
1 0 1 0.17 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
1 0 1 0.17 0 0
CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO
1 0 1 0.17 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC
1 0 1 0.17 0 0
Severe left ventricular systolic dysfunction
1 0 1 0.17 0 0