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: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges
52 0 1 1.4E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs
51 0 1 1.4E-03 0 0
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly
51 0 1 1.4E-03 0 0
CUI: C0427144
Disease: Toe-walking gait
Toe-walking gait
50 0 1 1.4E-03 0 0
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis
50 0 1 1.4E-03 0 0
CUI: C0431890
Disease: Hypoplasia of thumb
Hypoplasia of thumb
49 0 1 1.4E-03 0 0
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness
49 0 1 1.4E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 1 1.4E-03 0 0
CUI: C0035021
Disease: Relapsing Fever
Relapsing Fever
48 0 1 1.4E-03 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive
48 0 1 1.4E-03 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5
48 0 1 1.4E-03 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 0 1 1.4E-03 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy
46 0 1 1.4E-03 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility
45 0 1 1.4E-03 0 0
CUI: C1837402
Disease: Flat occiput
Flat occiput
45 0 1 1.4E-03 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1
45 0 1 1.4E-03 0 0
CUI: C0015930
Disease: Fetal Distress
Fetal Distress
44 0 1 1.4E-03 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon
44 0 1 1.4E-03 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity
43 0 1 1.4E-03 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 1 1.4E-03 0 0
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
42 0 1 1.4E-03 0 0
Thyroid stimulating hormone measurement
42 0 1 1.4E-03 0 0
CUI: C0234860
Disease: Weak cry
Weak cry
42 0 1 1.4E-03 0 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
42 0 1 1.4E-03 0 0
CUI: C0426818
Disease: Thin rib
Thin rib
42 0 1 1.4E-03 0 0