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: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction
22 0 10 0.14 0 0
CUI: C3160712
Disease: Palpitations, CTCAE
Palpitations, CTCAE
64 0 15 0.14 0 0
CUI: C1527344
Disease: Dysphonia
Dysphonia
77 0 16 0.13 0 0
CUI: C0029121
Disease: Oppositional Defiant Disorder
Oppositional Defiant Disorder
27 9 10 0.13 1 9.1E-02
CUI: C0030252
Disease: Palpitations
Palpitations
70 0 15 0.13 0 0
CUI: C1704374
Disease: Carcinoma of Endocrine Gland
Carcinoma of Endocrine Gland
22 0 9 0.12 0 0
CUI: C1857175
Disease: Episodic hypertension
Episodic hypertension
8 0 7 0.12 0 0
CUI: C0221154
Disease: Paroxysmal hypertension
Paroxysmal hypertension
9 0 7 0.11 0 0
CUI: C0031212
Disease: Personality Disorders
Personality Disorders
49 0 11 0.11 0 0
Bilateral pheochromocytoma and islet cell adenoma of the pancreas
10 0 7 0.11 0 0
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder
40 0 10 0.11 0 0
CUI: C0003076
Disease: Aniridia
Aniridia
83 0 14 0.11 0 0
CUI: C0016382
Disease: Flushing
Flushing
83 0 14 0.11 0 0
CUI: C0039231
Disease: Tachycardia
Tachycardia
73 0 13 0.11 0 0
CUI: C0012734
Disease: Disruptive Behavior Disorder
Disruptive Behavior Disorder
13 0 7 0.11 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor
57 0 11 0.10 0 0
CUI: C1333993
Disease: hereditary paraganglioma
hereditary paraganglioma
15 0 7 0.10 0 0
CUI: C0035067
Disease: Renal Artery Stenosis
Renal Artery Stenosis
37 0 9 0.10 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired
60 0 11 0.10 0 0
CUI: C0522254
Disease: Analgesic Overuse Headache
Analgesic Overuse Headache
28 0 8 0.10 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease
51 0 10 1.0E-01 0 0
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
175 101 21 9.9E-02 1 9.7E-03
Adult attention deficit hyperactivity disorder
20 0 7 9.7E-02 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism
33 0 8 9.5E-02 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 0 10 9.4E-02 0 0