Source: INFERRED ×
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: C0432333
Disease: Abnormal dermatoglyphic pattern
Abnormal dermatoglyphic pattern 		42 0 1 2.4E-02 0 0
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 1 9.1E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		93 0 1 1.1E-02 0 0
CUI: C2674737
Disease: Abnormality of finger
Abnormality of finger 		7 0 1 0.14 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		170 0 1 5.9E-03 0 0
CUI: C2674738
Disease: Abnormality of toe
Abnormality of toe 		6 0 1 0.17 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		122 0 1 8.2E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		38 0 1 2.6E-02 0 0
CUI: C0027859
Disease: Acoustic Neuroma
Acoustic Neuroma 		3 0 1 0.33 0 0
CUI: C0158486
Disease: Acquired genu recurvatum
Acquired genu recurvatum 		23 0 1 4.3E-02 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		135 0 1 7.4E-03 0 0
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly 		26 0 1 3.8E-02 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		136 390 1 7.4E-03 1 2.6E-03
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas 		38 114 1 2.6E-02 1 8.8E-03
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate 		16 96 1 6.2E-02 1 1.0E-02
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
Adenoid Cystic Carcinoma 		11 27 1 9.1E-02 1 3.7E-02
CUI: C0002170
Disease: Alopecia
Alopecia 		261 0 1 3.8E-03 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		407 0 1 2.5E-03 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		64 0 1 1.6E-02 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 1 8.6E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 9.3E-03 0 0
CUI: C0750929
Disease: Arnold-Chiari Malformation, Type I
Arnold-Chiari Malformation, Type I 		14 0 1 7.1E-02 0 0
CUI: C4022025
Disease: Asymmetric growth
Asymmetric growth 		6 0 1 0.17 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		250 0 1 4.0E-03 0 0
CUI: C0264172
Disease: Barrel chest
Barrel chest 		18 0 1 5.6E-02 0 0