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: C1970479
Disease: Branchiootorenal Syndrome 2
Branchiootorenal Syndrome 2
4 0 4 0.44 0 0
Abnormality of the middle ear ossicles
5 1 4 0.40 1 6.2E-02
CUI: C4551702
Disease: Branchiootorenal Syndrome 1
Branchiootorenal Syndrome 1
5 0 4 0.40 0 0
CUI: C1861544
Disease: Lower lip pit
Lower lip pit
3 0 3 0.33 0 0
CUI: C4021154
Disease: Enlarged cochlear aqueduct
Enlarged cochlear aqueduct
3 0 3 0.33 0 0
CUI: C0266092
Disease: Congenital lip pits
Congenital lip pits
4 0 3 0.30 0 0
CUI: C1858567
Disease: Abnormal lacrimal duct morphology
Abnormal lacrimal duct morphology
4 0 3 0.30 0 0
CUI: C0341059
Disease: Lip pit
Lip pit
14 0 5 0.28 0 0
CUI: C2676973
Disease: Dilatated internal auditory canal
Dilatated internal auditory canal
7 2 3 0.23 1 5.9E-02
CUI: C2676974
Disease: Hypoplasia of the cochlea
Hypoplasia of the cochlea
7 0 3 0.23 0 0
CUI: C1847604
Disease: Van der Woude syndrome 2
Van der Woude syndrome 2
2 0 2 0.22 0 0
CUI: C1862052
Disease: Gustatory lacrimation
Gustatory lacrimation
2 0 2 0.22 0 0
CUI: C1867020
Disease: SCALP-EAR-NIPPLE SYNDROME
SCALP-EAR-NIPPLE SYNDROME
2 0 2 0.22 0 0
ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT
2 0 2 0.22 0 0
CUI: C4551864
Disease: VAN DER WOUDE SYNDROME 1
VAN DER WOUDE SYNDROME 1
2 0 2 0.22 0 0
CUI: C0265234
Disease: Branchio-Oto-Renal Syndrome
Branchio-Oto-Renal Syndrome
14 0 4 0.21 0 0
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
3 0 2 0.20 0 0
CUI: C1865143
Disease: BRANCHIOOTIC SYNDROME 1
BRANCHIOOTIC SYNDROME 1
3 0 2 0.20 0 0
CUI: C0006131
Disease: Branchioma
Branchioma
10 0 3 0.19 0 0
CUI: C4021762
Disease: Abnormality of the cerebrum
Abnormality of the cerebrum
4 0 2 0.18 0 0
Incomplete partition of the cochlea type II
4 0 2 0.18 0 0
CUI: C0149772
Disease: Abnormal salivary gland morphology
Abnormal salivary gland morphology
5 0 2 0.17 0 0
CUI: C1852759
Disease: Papillorenal syndrome
Papillorenal syndrome
5 0 2 0.17 0 0
Morphological abnormality of the middle ear
6 0 2 0.15 0 0
CUI: C4273131
Disease: Branchiootic syndrome
Branchiootic syndrome
6 0 2 0.15 0 0