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: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0 427 0 0 1 2.2E-03
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement
0 33 0 0 1 1.9E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
147 0 1 1.6E-03 0 0
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
147 0 1 1.6E-03 0 0
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
147 0 1 1.6E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 1 1.6E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness
112 0 1 1.7E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 0 1 1.8E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling
95 0 1 1.8E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls
94 0 1 1.8E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 1 1.8E-03 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
80 0 1 1.8E-03 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia
77 0 1 1.8E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance
76 0 1 1.8E-03 0 0
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic
75 0 1 1.8E-03 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement
75 422 1 1.8E-03 1 2.3E-03
QT interval feature (observable entity)
75 0 1 1.8E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia
75 0 1 1.8E-03 0 0
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy
74 0 1 1.8E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact
73 0 1 1.8E-03 0 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency
71 0 1 1.8E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 1 1.9E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result
65 0 1 1.9E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance
65 0 1 1.9E-03 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor
62 0 1 1.9E-03 0 0