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: C0263472
Disease: Bromhidrosis
Bromhidrosis 		0 2 0 0 1 1.7E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 3 3.5E-02
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 1.7E-02
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.5E-03 0 0
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		134 0 1 1.6E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 1.6E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 1.6E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 1.6E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		100 0 1 1.6E-03 0 0
CUI: C0085583
Disease: Choreoathetosis
Choreoathetosis 		94 0 1 1.7E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.7E-03 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 1 1.7E-03 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		86 0 1 1.7E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 1.7E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.7E-03 0 0
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		82 0 1 1.7E-03 0 0
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		82 0 1 1.7E-03 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 1 1.7E-03 0 0
CUI: C1843156
Disease: Progressive sensorineural hearing impairment
Progressive sensorineural hearing impairment 		78 0 1 1.7E-03 0 0
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		77 0 1 1.7E-03 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement 		75 0 1 1.7E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 1.7E-03 0 0
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		74 0 1 1.7E-03 0 0
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		74 0 1 1.7E-03 0 0
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		69 0 1 1.7E-03 0 0