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: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 1.1E-03 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia 		39 0 1 1.1E-03 0 0
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		39 0 1 1.1E-03 0 0
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		39 0 1 1.1E-03 0 0
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		39 0 1 1.1E-03 0 0
CUI: C0263454
Disease: Chloracne
Chloracne 		38 0 1 1.1E-03 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 1 1.1E-03 0 0
CUI: C1859461
Disease: Femoral bowing
Femoral bowing 		38 0 1 1.1E-03 0 0
CUI: C0038238
Disease: Steatorrhea
Steatorrhea 		37 0 1 1.1E-03 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 1.1E-03 0 0
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		37 0 1 1.1E-03 0 0
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		36 0 1 1.1E-03 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 1 1.1E-03 0 0
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		36 0 1 1.1E-03 0 0
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		36 0 1 1.1E-03 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 1 1.1E-03 0 0
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		35 0 1 1.1E-03 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 1 1.1E-03 0 0
CUI: C0344559
Disease: Irido-corneo-trabecular dysgenesis (disorder)
Irido-corneo-trabecular dysgenesis (disorder) 		35 0 1 1.1E-03 0 0
CUI: C1833144
Disease: Slender long bone
Slender long bone 		35 0 1 1.1E-03 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 1 1.1E-03 0 0
CUI: C3149631
Disease: MELORHEOSTOSIS, ISOLATED
MELORHEOSTOSIS, ISOLATED 		35 0 1 1.1E-03 0 0
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly 		34 0 1 1.1E-03 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray 		34 0 1 1.1E-03 0 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice 		33 0 1 1.1E-03 0 0