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: C4021794
Disease: Abnormality of the adrenal glands
Abnormality of the adrenal glands 		10 0 2 8.3E-02 0 0
CUI: C1849510
Disease: Prenatal movement abnormality
Prenatal movement abnormality 		11 0 2 8.0E-02 0 0
CUI: C1851792
Disease: Aplasia/Hypoplasia of the earlobes
Aplasia/Hypoplasia of the earlobes 		11 0 2 8.0E-02 0 0
CUI: C4048199
Disease: Ulnar deviation of the hand or of fingers of the hand
Ulnar deviation of the hand or of fingers of the hand 		11 0 2 8.0E-02 0 0
CUI: C0037301
Disease: Skin Wrinkling
Skin Wrinkling 		12 0 2 7.7E-02 0 0
CUI: C1446712
Disease: Overlapping fingers
Overlapping fingers 		27 0 3 7.5E-02 0 0
CUI: C4551936
Disease: Anal Stenosis, CTCAE
Anal Stenosis, CTCAE 		27 0 3 7.5E-02 0 0
CUI: C0152419
Disease: Interrupted aortic arch
Interrupted aortic arch 		13 0 2 7.4E-02 0 0
CUI: C4025663
Disease: Abnormality of tibia morphology
Abnormality of tibia morphology 		13 0 2 7.4E-02 0 0
CUI: C0262374
Disease: Stricture of anus
Stricture of anus 		28 0 3 7.3E-02 0 0
CUI: C0151491
Disease: Congenital musculoskeletal anomalies
Congenital musculoskeletal anomalies 		14 0 2 7.1E-02 0 0
CUI: C0231678
Disease: Ulnar deviation of the wrist
Ulnar deviation of the wrist 		14 0 2 7.1E-02 0 0
CUI: C4021801
Disease: Lacrimation abnormality
Lacrimation abnormality 		29 0 3 7.1E-02 0 0
CUI: C0341787
Disease: Bifid scrotum
Bifid scrotum 		30 0 3 7.0E-02 0 0
CUI: C1282609
Disease: Granulocytosis
Granulocytosis 		15 0 2 6.9E-02 0 0
CUI: C0231679
Disease: Ulnar deviation of the fingers
Ulnar deviation of the fingers 		31 0 3 6.8E-02 0 0
CUI: C0332878
Disease: Congenital contracture
Congenital contracture 		31 0 3 6.8E-02 0 0
CUI: C1837835
Disease: Bilateral talipes equinovarus
Bilateral talipes equinovarus 		16 0 2 6.7E-02 0 0
CUI: C2931150
Disease: Synostotic Anterior Plagiocephaly
Synostotic Anterior Plagiocephaly 		16 0 2 6.7E-02 0 0
CUI: C4025250
Disease: Abnormal sacrum morphology
Abnormal sacrum morphology 		17 0 2 6.5E-02 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 6.2E-02 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 2 1 6.2E-02 1 0.33
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 6.2E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 6.2E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 6.2E-02 0 0