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: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 2.7E-03 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 1 2.7E-03 0 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		92 0 1 2.7E-03 0 0
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 0 1 2.7E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 2.7E-03 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 1 2.8E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 1 2.8E-03 0 0
CUI: C1853738
Disease: Long eyelashes
Long eyelashes 		83 0 1 2.8E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 2.8E-03 0 0
CUI: C0236733
Disease: Amphetamine-Related Disorders
Amphetamine-Related Disorders 		78 0 1 2.8E-03 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		78 0 1 2.8E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		76 0 1 2.8E-03 0 0
CUI: C0236807
Disease: Amphetamine Abuse
Amphetamine Abuse 		75 0 1 2.8E-03 0 0
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 		74 0 1 2.8E-03 0 0
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		70 0 1 2.9E-03 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 1 2.9E-03 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 1 2.9E-03 0 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		68 0 1 2.9E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 2.9E-03 0 0
CUI: C1862095
Disease: Bilateral single transverse palmar creases
Bilateral single transverse palmar creases 		65 0 1 2.9E-03 0 0
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		63 0 1 2.9E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 1 2.9E-03 0 0
CUI: C0401151
Disease: Chronic diarrhea
Chronic diarrhea 		62 0 1 2.9E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 2.9E-03 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 1 3.0E-03 0 0