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: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 1 6.5E-04 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign
54 0 1 6.5E-04 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 6.5E-04 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges
52 0 1 6.5E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 1 6.5E-04 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies
44 0 1 6.5E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance
44 0 1 6.5E-04 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 1 6.5E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 1 6.6E-04 0 0
Impaired nasal mucociliary clearance
41 0 1 6.6E-04 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia
39 0 1 6.6E-04 0 0
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
39 0 1 6.6E-04 0 0
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
39 0 1 6.6E-04 0 0
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
39 0 1 6.6E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 1 6.6E-04 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
39 0 1 6.6E-04 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy
38 0 1 6.6E-04 0 0
CUI: C0018810
Disease: heart rate
heart rate
36 0 1 6.6E-04 0 0
Decreased activity of the pyruvate dehydrogenase complex
35 0 1 6.6E-04 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI
35 0 1 6.6E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis
35 0 1 6.6E-04 0 0
CUI: C0020580
Disease: Hypesthesia
Hypesthesia
33 0 1 6.6E-04 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense
33 0 1 6.6E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia
33 0 1 6.6E-04 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination
32 0 1 6.6E-04 0 0