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: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 2.1E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result 		65 0 1 2.1E-03 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 1 2.1E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 2.1E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 2.1E-03 0 0
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria 		60 0 1 2.1E-03 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 1 2.1E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 2.1E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 2.1E-03 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve 		59 0 1 2.1E-03 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		59 0 1 2.1E-03 0 0
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		57 0 1 2.1E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 2.1E-03 0 0
CUI: C0424166
Disease: Social Anxiety
Social Anxiety 		57 0 1 2.1E-03 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		57 0 1 2.1E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 2.1E-03 0 0
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		56 0 1 2.1E-03 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 1 2.1E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 2.1E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem 		55 0 1 2.1E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 2.1E-03 0 0
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies 		53 0 1 2.2E-03 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 1 2.2E-03 0 0
CUI: C0342776
Disease: Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency 		51 0 1 2.2E-03 0 0
CUI: C0427144
Disease: Toe-walking gait
Toe-walking gait 		50 0 1 2.2E-03 0 0