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 3 2.7E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 2 7.9E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 6.1E-03 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 1 2.9E-04 0 0
CUI: C0002871
Disease: Anemia
Anemia
847 0 2 2.4E-03 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly
59 0 3 5.0E-02 0 0
CUI: C0003119
Disease: Anophthalmos
Anophthalmos
89 0 3 3.3E-02 0 0
CUI: C0003578
Disease: Apnea
Apnea
262 0 4 1.5E-02 0 0
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
2006 0 1 5.0E-04 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 4 4.6E-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 4 6.7E-03 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness
16 0 1 5.3E-02 0 0
CUI: C0007138
Disease: Carcinoma, Transitional Cell
Carcinoma, Transitional Cell
623 0 1 1.6E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
441 0 1 2.3E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 4 6.5E-03 0 0
Congenital ocular coloboma (disorder)
129 0 2 1.5E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital
63 0 4 6.3E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 4 5.5E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome
137 0 4 2.9E-02 0 0
CUI: C0012817
Disease: Diverticulum
Diverticulum
12 0 1 6.7E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism
1261 0 4 3.2E-03 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia
93 0 4 4.3E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
33 0 2 5.7E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
121 0 1 8.1E-03 0 0