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: C4476749
Disease: Crazy paving pattern on pulmonary HRCT
Crazy paving pattern on pulmonary HRCT 		3 0 3 0.33 0 0
CUI: C4476917
Disease: Elevated carcinoembryonic antigen level
Elevated carcinoembryonic antigen level 		4 0 3 0.30 0 0
CUI: C2931035
Disease: Pulmonary alveolar proteinosis, congenital
Pulmonary alveolar proteinosis, congenital 		5 0 3 0.27 0 0
CUI: C4022660
Disease: Autoimmune antibody positivity
Autoimmune antibody positivity 		5 0 3 0.27 0 0
CUI: C4281786
Disease: Presence of foam cells
Presence of foam cells 		5 0 3 0.27 0 0
CUI: C4023112
Disease: Acute infectious pneumonia
Acute infectious pneumonia 		7 0 3 0.23 0 0
CUI: C0009176
Disease: Cocaine intoxication
Cocaine intoxication 		1 0 1 0.11 0 0
CUI: C0020529
Disease: Hypersomnia with Periodic Respiration
Hypersomnia with Periodic Respiration 		1 0 1 0.11 0 0
CUI: C0240302
Disease: Masseter Muscle Spasm
Masseter Muscle Spasm 		1 0 1 0.11 0 0
CUI: C0268248
Disease: Niemann-Pick Disease, Type E
Niemann-Pick Disease, Type E 		1 0 1 0.11 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 0.11 0 0
CUI: C0338495
Disease: Sleep Apnea, Mixed Central and Obstructive
Sleep Apnea, Mixed Central and Obstructive 		1 0 1 0.11 0 0
CUI: C0343495
Disease: Lockjaw
Lockjaw 		1 0 1 0.11 0 0
CUI: C0473223
Disease: Aluminum intoxication
Aluminum intoxication 		1 0 1 0.11 0 0
CUI: C0476337
Disease: Blood gases abnormal
Blood gases abnormal 		1 0 1 0.11 0 0
CUI: C0520758
Disease: Prolonged neuromuscular block
Prolonged neuromuscular block 		1 0 1 0.11 0 0
CUI: C0541957
Disease: Fasciculation, Skeletal Muscle
Fasciculation, Skeletal Muscle 		1 0 1 0.11 0 0
CUI: C0751144
Disease: Fasciculation, Benign
Fasciculation, Benign 		1 0 1 0.11 0 0
CUI: C1283400
Disease: Butyrylcholinesterase deficiency
Butyrylcholinesterase deficiency 		1 0 1 0.11 0 0
CUI: C1622434
Disease: Suxamethonium sensitivity
Suxamethonium sensitivity 		1 0 1 0.11 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 0.11 0 0
CUI: C1837615
Disease: Ciliary Dyskinesia, Primary, 5
Ciliary Dyskinesia, Primary, 5 		1 0 1 0.11 0 0
CUI: C1843428
Disease: Diffuse reticular or finely nodular infiltrations
Diffuse reticular or finely nodular infiltrations 		1 0 1 0.11 0 0
CUI: C1856974
Disease: PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder)
PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder) 		1 0 1 0.11 0 0
CUI: C1857762
Disease: Olivopontocerebellar hypoplasia, fetal-onset
Olivopontocerebellar hypoplasia, fetal-onset 		1 0 1 0.11 0 0