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: C0266383
Disease: Uterine Anomalies
Uterine Anomalies
35 1 21 0.23 1 0.20
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
32 0 14 0.15 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia
104 0 22 0.14 0 0
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
187 23 32 0.14 1 3.7E-02
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 25 0.13 0 0
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
96 0 20 0.13 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis
12 0 10 0.13 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
102 0 20 0.13 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch
13 0 10 0.12 0 0
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidney
121 0 22 0.12 0 0
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association
25 0 11 0.12 0 0
CUI: C0032209
Disease: Platybasia
Platybasia
18 0 10 0.12 0 0
CUI: C0243002
Disease: Tricuspid Atresia
Tricuspid Atresia
18 0 10 0.12 0 0
CUI: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele
9 0 9 0.12 0 0
CUI: C0264303
Disease: Laryngomalacia
Laryngomalacia
67 0 15 0.12 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
384 0 47 0.11 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 9 0.11 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils
12 0 9 0.11 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag
53 0 13 0.11 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
225 21 30 0.11 1 4.0E-02
CUI: C1301937
Disease: Talipes
Talipes
74 0 15 0.11 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus
34 0 11 0.11 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
85 0 16 0.11 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly
75 0 15 0.11 0 0
CUI: C1837731
Disease: Overfolded helix
Overfolded helix
46 0 12 0.11 0 0