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: C1839546
Disease: Microretrognathia
Microretrognathia
53 0 1 6.6E-04 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux
50 0 1 6.6E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus
48 0 1 6.6E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 0 1 6.7E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 1 6.7E-04 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies
44 0 1 6.7E-04 0 0
Atresia of the external auditory canal
44 0 1 6.7E-04 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 1 6.7E-04 0 0
Complex partial seizure with impairment of consciousness
41 0 1 6.7E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia
41 0 1 6.7E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity
41 0 1 6.7E-04 0 0
CUI: C4082169
Disease: Metatarsus Varus
Metatarsus Varus
41 0 1 6.7E-04 0 0
Impaired nasal mucociliary clearance
41 0 1 6.7E-04 0 0
CUI: C0266610
Disease: Preauricular dimple
Preauricular dimple
40 0 1 6.7E-04 0 0
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 6.7E-04 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block
39 0 1 6.7E-04 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness
39 0 1 6.7E-04 0 0
Abnormal mitochondria in muscle tissue
39 0 1 6.7E-04 0 0
CUI: C1836696
Disease: Lower limb hyperreflexia
Lower limb hyperreflexia
38 0 1 6.7E-04 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy
38 0 1 6.7E-04 0 0
CUI: C0002453
Disease: Amenorrhea
Amenorrhea
37 0 1 6.7E-04 0 0
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
37 0 1 6.7E-04 0 0
CUI: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs
37 0 1 6.7E-04 0 0
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
37 0 1 6.7E-04 0 0
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
36 0 1 6.7E-04 0 0