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: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 5.9E-03
CUI: C0424678
Disease: Lean body mass
Lean body mass 		144 0 1 1.9E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 2.0E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 2.0E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.0E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 2.1E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 2.1E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 1 2.1E-03 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 1 2.1E-03 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 0 1 2.1E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 2.2E-03 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		90 0 1 2.2E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 2.2E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 2.2E-03 0 0
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		85 0 1 2.2E-03 0 0
CUI: C1853738
Disease: Long eyelashes
Long eyelashes 		83 0 1 2.2E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 2.2E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 2.2E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		82 0 1 2.2E-03 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		78 0 1 2.2E-03 0 0
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		77 0 1 2.2E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 2.2E-03 0 0
CUI: C0423757
Disease: Thin skin
Thin skin 		77 0 1 2.2E-03 0 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency 		71 0 1 2.2E-03 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 0 1 2.3E-03 0 0