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: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 1 7.5E-04 0 0
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval
38 0 1 7.6E-04 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running
38 0 1 7.6E-04 0 0
CUI: C0010093
Disease: Corpus Luteum Cyst
Corpus Luteum Cyst
36 0 1 7.6E-04 0 0
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis
36 0 1 7.6E-04 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome
36 0 1 7.6E-04 0 0
CUI: C0744356
Disease: Abnormality of the genital system
Abnormality of the genital system
36 0 1 7.6E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 7.6E-04 0 0
CUI: C0240991
Disease: Ataxia, Sensory
Ataxia, Sensory
35 0 1 7.6E-04 0 0
Fukuyama Type Congenital Muscular Dystrophy
35 0 1 7.6E-04 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space
35 0 1 7.6E-04 0 0
CUI: C4317124
Disease: Polynesian Bronchiectasis
Polynesian Bronchiectasis
35 0 1 7.6E-04 0 0
CUI: C0038506
Disease: Stuttering
Stuttering
34 0 1 7.6E-04 0 0
CUI: C0598275
Disease: Diffuse cerebral atrophy
Diffuse cerebral atrophy
34 0 1 7.6E-04 0 0
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait
34 0 1 7.6E-04 0 0
Moderate sensorineural hearing impairment
34 0 1 7.6E-04 0 0
CUI: C0432355
Disease: Hypoplasia of nipple
Hypoplasia of nipple
33 0 1 7.6E-04 0 0
CUI: C0558845
Disease: Reflex, Ankle, Absent
Reflex, Ankle, Absent
33 0 1 7.6E-04 0 0
CUI: C1261470
Disease: Congenital meningocele
Congenital meningocele
33 0 1 7.6E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia
33 0 1 7.6E-04 0 0
CUI: C0271683
Disease: Polyneuropathy, Motor
Polyneuropathy, Motor
32 0 1 7.6E-04 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
32 0 1 7.6E-04 0 0
CUI: C4021620
Disease: Clinodactyly of the 2nd toe
Clinodactyly of the 2nd toe
32 0 1 7.6E-04 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination
32 0 1 7.6E-04 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur
31 0 1 7.6E-04 0 0