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: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 1 1.1E-03 0 0
CUI: C4025723
Disease: Abnormal upper motor neuron morphology
Abnormal upper motor neuron morphology 		20 0 1 5.0E-02 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		171 0 1 5.8E-03 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		2438 0 1 4.1E-04 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		656 0 1 1.5E-03 0 0
CUI: C4017118
Disease: ADULT POLYGLUCOSAN BODY NEUROPATHY
ADULT POLYGLUCOSAN BODY NEUROPATHY 		1 0 1 1.00 0 0
CUI: C0085623
Disease: Akinesia
Akinesia 		43 0 1 2.3E-02 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 0 1 5.1E-03 0 0
CUI: C0003962
Disease: Ascites
Ascites 		198 0 1 5.1E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.2E-03 0 0
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas 		1408 0 1 7.1E-04 0 0
CUI: C1305855
Disease: Body mass index
Body mass index 		1014 0 1 9.9E-04 0 0
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		4081 0 1 2.5E-04 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		925 0 1 1.1E-03 0 0
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 0 1 1.3E-03 0 0
CUI: C0342790
Disease: Carnitine palmitoyl transferase 2 deficiency
Carnitine palmitoyl transferase 2 deficiency 		11 0 1 9.1E-02 0 0
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		1658 0 1 6.0E-04 0 0
CUI: C0795956
Disease: Chylomicron retention disease
Chylomicron retention disease 		10 0 1 1.0E-01 0 0
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		919 0 1 1.1E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 1.6E-02 0 0
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		65 0 1 1.5E-02 0 0
CUI: C0497327
Disease: Dementia
Dementia 		816 0 1 1.2E-03 0 0
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		2803 0 1 3.6E-04 0 0
CUI: C0032708
Disease: Disorders of Porphyrin Metabolism
Disorders of Porphyrin Metabolism 		26 0 1 3.8E-02 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 1 1.2E-02 0 0