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: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 1 9.1E-04 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 6.2E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta
61 0 1 1.6E-02 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly
59 0 1 1.7E-02 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos
89 0 1 1.1E-02 0 0
CUI: C0003578
Disease: Apnea
Apnea
262 0 1 3.8E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 1 1.2E-03 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
1112 0 1 9.0E-04 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.7E-03 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness
16 0 1 5.9E-02 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 1 5.3E-04 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 1 1.6E-03 0 0
Congenital ocular coloboma (disorder)
129 0 1 7.7E-03 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital
63 0 1 1.6E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 1 1.4E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome
137 0 1 7.2E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 1 7.9E-04 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia
93 0 1 1.1E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
33 0 1 2.9E-02 0 0
CUI: C0014394
Disease: Enuresis
Enuresis
27 0 1 3.6E-02 0 0
CUI: C0015230
Disease: Exanthema
Exanthema
251 0 1 4.0E-03 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
400 0 1 2.5E-03 0 0
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
1037 0 1 9.6E-04 0 0
CUI: C0016049
Disease: Fibromatosis, Gingival
Fibromatosis, Gingival
20 0 1 4.8E-02 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
1760 0 1 5.7E-04 0 0