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: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
1 0 1 1.00 0 0
CUI: C1833691
Disease: Otofaciocervical Syndrome
Otofaciocervical Syndrome
2 0 1 0.50 0 0
CUI: C1865143
Disease: BRANCHIOOTIC SYNDROME 1
BRANCHIOOTIC SYNDROME 1
2 7 1 0.50 2 0.25
ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT
2 0 1 0.50 0 0
CUI: C4273131
Disease: Branchiootic syndrome
Branchiootic syndrome
2 0 1 0.50 0 0
CUI: C0265234
Disease: Branchio-Oto-Renal Syndrome
Branchio-Oto-Renal Syndrome
4 0 1 0.25 0 0
CUI: C0376524
Disease: Branchio-Oculo-Facial Syndrome
Branchio-Oculo-Facial Syndrome
4 0 1 0.25 0 0
CUI: C1970479
Disease: Branchiootorenal Syndrome 2
Branchiootorenal Syndrome 2
4 0 1 0.25 0 0
CUI: C4551702
Disease: Branchiootorenal Syndrome 1
Branchiootorenal Syndrome 1
4 22 1 0.25 2 8.7E-02
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association
10 0 1 1.0E-01 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
11 0 1 9.1E-02 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears
41 0 1 2.4E-02 0 0
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
44 0 1 2.3E-02 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
98 0 1 1.0E-02 0 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
156 0 1 6.4E-03 0 0