Source: ALL
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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.4E-03
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 3.4E-03
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 3.4E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 3.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.3E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.4E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 3.4E-03
CUI: C0476482
Disease: Restlessness and agitation
Restlessness and agitation 		0 1 0 0 1 3.4E-03
CUI: C0751360
Disease: Becker Generalized Myotonia
Becker Generalized Myotonia 		0 67 0 0 3 8.3E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.4E-03
CUI: C1456145
Disease: Dental caries of smooth surface
Dental caries of smooth surface 		0 12 0 0 1 3.2E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 3.4E-03
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 3.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 2 6.7E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.4E-03
CUI: C4022169
Disease: EMG: myotonic discharges
EMG: myotonic discharges 		0 3 0 0 1 3.3E-03
CUI: C4022683
Disease: Myotonia of the upper limb
Myotonia of the upper limb 		0 2 0 0 1 3.4E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.4E-03
CUI: C4546209
Disease: Chronic pain following trauma
Chronic pain following trauma 		0 1 0 0 1 3.4E-03
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		41 0 1 5.7E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 5.7E-04 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		41 0 1 5.7E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 5.7E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 5.7E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis 		35 0 1 5.7E-04 0 0