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: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 6.1E-02
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 2.9E-02
CUI: C3553462
Disease: INFLUENZA, SEVERE, SUSCEPTIBILITY TO
INFLUENZA, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 3.0E-02
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 9.0E-04 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 9.1E-04 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 9.1E-04 0 0
CUI: C0426817
Disease: Short ribs
Short ribs 		60 0 1 9.2E-04 0 0
CUI: C0241210
Disease: Speech Delay
Speech Delay 		58 0 1 9.2E-04 0 0
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		52 0 1 9.2E-04 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		50 0 1 9.3E-04 0 0
CUI: C0427144
Disease: Toe-walking gait
Toe-walking gait 		50 0 1 9.3E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 9.3E-04 0 0
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		46 0 1 9.3E-04 0 0
CUI: C0263490
Disease: Brittle hair
Brittle hair 		45 0 1 9.3E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 9.3E-04 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		44 0 1 9.3E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 9.3E-04 0 0
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 0 1 9.3E-04 0 0
CUI: C1854912
Disease: Short long bone
Short long bone 		42 0 1 9.3E-04 0 0
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair 		42 0 1 9.3E-04 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 0 1 9.3E-04 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 9.3E-04 0 0
CUI: C0877165
Disease: Short phalanx of finger
Short phalanx of finger 		41 0 1 9.3E-04 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia 		41 0 1 9.3E-04 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 9.3E-04 0 0