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: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.2E-03 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 1 1.2E-03 0 0
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		44 0 1 1.2E-03 0 0
CUI: C0240735
Disease: Personality Change
Personality Change 		43 0 1 1.2E-03 0 0
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 0 1 1.2E-03 0 0
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair 		42 0 1 1.2E-03 0 0
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		41 0 1 1.2E-03 0 0
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney 		41 0 1 1.2E-03 0 0
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		41 0 1 1.2E-03 0 0
CUI: C1285654
Disease: Memory performance
Memory performance 		40 0 1 1.2E-03 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 1 1.2E-03 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		39 0 1 1.2E-03 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness 		39 0 1 1.2E-03 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 1 1.2E-03 0 0
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair 		39 0 1 1.2E-03 0 0
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		39 0 1 1.2E-03 0 0
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval 		38 0 1 1.2E-03 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 1 1.2E-03 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 0 1 1.2E-03 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 1.2E-03 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 1 1.2E-03 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 1.2E-03 0 0
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk 		37 0 1 1.2E-03 0 0
CUI: C0018810
Disease: heart rate
heart rate 		36 0 1 1.2E-03 0 0
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		36 0 1 1.2E-03 0 0