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: C1321422
Disease: Monoblastic leukemia
Monoblastic leukemia
14 0 2 7.1E-02 0 0
Paroxysmal kinesigenic choreoathetosis
14 0 2 7.1E-02 0 0
CUI: C0752210
Disease: Dyskinesias, Paroxysmal
Dyskinesias, Paroxysmal
15 0 2 6.9E-02 0 0
CUI: C0085435
Disease: Arthritis, Reactive
Arthritis, Reactive
63 0 5 6.8E-02 0 0
CUI: C0030196
Disease: Pain in limb
Pain in limb
16 5 2 6.7E-02 1 1.5E-02
CUI: C0221055
Disease: Paramyotonia Congenita (disorder)
Paramyotonia Congenita (disorder)
17 0 2 6.5E-02 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output
1 0 1 6.2E-02 0 0
Pulmonary embolism with pulmonary infarction
1 0 1 6.2E-02 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis
1 0 1 6.2E-02 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia
1 0 1 6.2E-02 0 0
CUI: C0332882
Disease: congenital obstruction
congenital obstruction
1 0 1 6.2E-02 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome
1 0 1 6.2E-02 0 0
Distal intestinal obstruction syndrome
1 0 1 6.2E-02 0 0
CUI: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia
1 0 1 6.2E-02 0 0
Type 2 diabetes mellitus without complication
1 0 1 6.2E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia
1 0 1 6.2E-02 0 0
CUI: C0600177
Disease: Low Cardiac Output Syndrome
Low Cardiac Output Syndrome
1 0 1 6.2E-02 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions
1 0 1 6.2E-02 0 0
CUI: C0751535
Disease: Syncope, Cardiogenic
Syncope, Cardiogenic
1 0 1 6.2E-02 0 0
CUI: C0856123
Disease: Myotonia aggravated
Myotonia aggravated
1 0 1 6.2E-02 0 0
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration
1 0 1 6.2E-02 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps
1 0 1 6.2E-02 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection
1 0 1 6.2E-02 0 0
CHOREOATHETOSIS/SPASTICITY, EPISODIC
1 0 1 6.2E-02 0 0
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
1 0 1 6.2E-02 0 0