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: C0014863
Disease: Esophageal spasm
Esophageal spasm 		6 0 1 5.9E-02 0 0
CUI: C4727182
Disease: Recurrent Cushing Disease
Recurrent Cushing Disease 		6 0 1 5.9E-02 0 0
CUI: C1336117
Disease: Stage IA Lung Adenocarcinoma AJCC v7
Stage IA Lung Adenocarcinoma AJCC v7 		7 0 1 5.6E-02 0 0
CUI: C1621719
Disease: Lymphoepithelioid lymphoma (clinical)
Lymphoepithelioid lymphoma (clinical) 		7 0 1 5.6E-02 0 0
CUI: C2697765
Disease: Interleukin 17 Measurement
Interleukin 17 Measurement 		7 0 1 5.6E-02 0 0
CUI: C0042035
Disease: Urination Disorders
Urination Disorders 		8 0 1 5.3E-02 0 0
CUI: C0334384
Disease: Infiltrating duct and lobular carcinoma
Infiltrating duct and lobular carcinoma 		8 0 1 5.3E-02 0 0
CUI: C0558916
Disease: Nasal and nasal-type NK/T-cell lymphoma
Nasal and nasal-type NK/T-cell lymphoma 		8 0 1 5.3E-02 0 0
CUI: C0600272
Disease: Morphine Abuse
Morphine Abuse 		8 0 1 5.3E-02 0 0
CUI: C1867403
Disease: Pyloric Stenosis, Infantile Hypertrophic 1
Pyloric Stenosis, Infantile Hypertrophic 1 		8 0 1 5.3E-02 0 0
CUI: C3146244
Disease: Alcohol Related Birth Defect
Alcohol Related Birth Defect 		8 0 1 5.3E-02 0 0
CUI: C2609059
Disease: Antisynthetase syndrome
Antisynthetase syndrome 		9 0 1 5.0E-02 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 1 5.0E-02 0 0
CUI: C0025265
Disease: Memory, Short-Term
Memory, Short-Term 		10 0 1 4.8E-02 0 0
CUI: C0085541
Disease: Epilepsy, Frontal Lobe
Epilepsy, Frontal Lobe 		10 0 1 4.8E-02 0 0
CUI: C0403670
Disease: Urinary incontinence of non-organic origin
Urinary incontinence of non-organic origin 		10 0 1 4.8E-02 0 0
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia 		11 0 1 4.5E-02 0 0
CUI: C0276093
Disease: edema disease
edema disease 		11 0 1 4.5E-02 0 0
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin 		11 0 1 4.5E-02 0 0
CUI: C3812396
Disease: Chronic idiopathic pulmonary fibrosis
Chronic idiopathic pulmonary fibrosis 		11 0 1 4.5E-02 0 0
CUI: C0206307
Disease: Canavan Disease
Canavan Disease 		12 0 1 4.3E-02 0 0
CUI: C0271738
Disease: Hypocortisolism secondary to another disorder
Hypocortisolism secondary to another disorder 		13 0 1 4.2E-02 0 0
CUI: C0338596
Disease: Spastic cerebral palsy
Spastic cerebral palsy 		13 0 1 4.2E-02 0 0
CUI: C0751197
Disease: Fulminant Hepatic Failure with Cerebral Edema
Fulminant Hepatic Failure with Cerebral Edema 		13 0 1 4.2E-02 0 0
CUI: C0751198
Disease: Hepatic Stupor
Hepatic Stupor 		13 0 1 4.2E-02 0 0