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: C0920209
Disease: Hypercapnic encephalopathy
Hypercapnic encephalopathy 		1 0 1 3.4E-02 0 0
CUI: C0948779
Disease: Gastrointestinal hypomotility
Gastrointestinal hypomotility 		1 0 1 3.4E-02 0 0
CUI: C1261120
Disease: Chronic bullous emphysema
Chronic bullous emphysema 		1 0 1 3.4E-02 0 0
CUI: C1266014
Disease: Canalicular adenoma
Canalicular adenoma 		1 0 1 3.4E-02 0 0
CUI: C1313961
Disease: Trichorrhexis nodosa syndrome
Trichorrhexis nodosa syndrome 		1 0 1 3.4E-02 0 0
CUI: C1332860
Disease: Cauda Equina Paraganglioma
Cauda Equina Paraganglioma 		1 0 1 3.4E-02 0 0
CUI: C1410087
Disease: Spine stiffness
Spine stiffness 		1 0 1 3.4E-02 0 0
CUI: C1837371
Disease: Sudden Infant Death with Dysgenesis of the Testes Syndrome
Sudden Infant Death with Dysgenesis of the Testes Syndrome 		1 0 1 3.4E-02 0 0
CUI: C1837379
Disease: Partial development of the penile shaft
Partial development of the penile shaft 		1 0 1 3.4E-02 0 0
CUI: C1837380
Disease: Dysplastic testes
Dysplastic testes 		1 0 1 3.4E-02 0 0
CUI: C1839727
Disease: Mental Retardation with Spastic Paraplegia
Mental Retardation with Spastic Paraplegia 		1 0 1 3.4E-02 0 0
CUI: C1842149
Disease: Spondyloepiphyseal Dysplasia, Kimberley Type
Spondyloepiphyseal Dysplasia, Kimberley Type 		1 0 1 3.4E-02 0 0
CUI: C1848901
Disease: TESTES, RUDIMENTARY
TESTES, RUDIMENTARY 		1 0 1 3.4E-02 0 0
CUI: C1853102
Disease: Cerebrooculofacioskeletal Syndrome 2
Cerebrooculofacioskeletal Syndrome 2 		1 0 1 3.4E-02 0 0
CUI: C1868633
Disease: Paragangliomas with Sensorineural Hearing Loss
Paragangliomas with Sensorineural Hearing Loss 		1 0 1 3.4E-02 0 0
CUI: C1960046
Disease: Mild persistent asthma
Mild persistent asthma 		1 0 1 3.4E-02 0 0
CUI: C1960052
Disease: Chronic hypercapnic respiratory failure
Chronic hypercapnic respiratory failure 		1 0 1 3.4E-02 0 0
CUI: C1970808
Disease: Xeroderma Pigmentosum B-Cockayne Syndrome
Xeroderma Pigmentosum B-Cockayne Syndrome 		1 0 1 3.4E-02 0 0
CUI: C2748544
Disease: Spondyloepimetaphyseal Dysplasia, Aggrecan Type
Spondyloepimetaphyseal Dysplasia, Aggrecan Type 		1 0 1 3.4E-02 0 0
CUI: C2751535
Disease: Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet
Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet 		1 0 1 3.4E-02 0 0
CUI: C2873755
Disease: Triple gene defect alpha thalassemia
Triple gene defect alpha thalassemia 		1 0 1 3.4E-02 0 0
CUI: C2930849
Disease: Von willebrand factor, deficiency
Von willebrand factor, deficiency 		1 0 1 3.4E-02 0 0
CUI: C3161173
Disease: Hemoglobin H Constant Spring
Hemoglobin H Constant Spring 		1 0 1 3.4E-02 0 0
CUI: C3161175
Disease: Hydrops fetalis due to alpha thalassemia
Hydrops fetalis due to alpha thalassemia 		1 0 1 3.4E-02 0 0
CUI: C3203502
Disease: Hyperactive delirium
Hyperactive delirium 		1 0 1 3.4E-02 0 0