Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Cryptophthalmos, Unilateral or Bilateral, Isolated
1 0 1 1.00 0 0
CUI: C4305274
Disease: Isolated cryptophthalmos
Isolated cryptophthalmos
1 0 1 1.00 0 0
CUI: C4540036
Disease: FRASER SYNDROME 2
FRASER SYNDROME 2
1 0 1 1.00 0 0
CUI: C1855425
Disease: Marles Greenberg Persaud syndrome
Marles Greenberg Persaud syndrome
3 0 1 0.33 0 0
CUI: C4024757
Disease: Malformed lacrimal duct
Malformed lacrimal duct
3 0 1 0.33 0 0
CUI: C4024773
Disease: Lacrimal duct aplasia
Lacrimal duct aplasia
3 0 1 0.33 0 0
CUI: C4303547
Disease: BNAR syndrome
BNAR syndrome
3 0 1 0.33 0 0
CUI: C4551480
Disease: FRASER SYNDROME 1
FRASER SYNDROME 1
3 0 1 0.33 0 0
CUI: C1844537
Disease: Cleft ala nasi
Cleft ala nasi
4 0 1 0.25 0 0
CUI: C4023812
Disease: Aplasia of the bladder
Aplasia of the bladder
4 0 1 0.25 0 0
CUI: C4025412
Disease: Midline nasal groove
Midline nasal groove
4 0 1 0.25 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos
5 1 1 0.20 1 1.00
CUI: C1857190
Disease: Wide pubic symphysis
Wide pubic symphysis
5 0 1 0.20 0 0
CUI: C0521622
Disease: Bilateral hydronephrosis
Bilateral hydronephrosis
6 0 1 0.17 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome
8 0 1 0.12 0 0
CUI: C0238394
Disease: Female Pseudohermaphroditism
Female Pseudohermaphroditism
10 0 1 1.0E-01 0 0
CUI: C0023075
Disease: Laryngostenosis
Laryngostenosis
11 0 1 9.1E-02 0 0
CUI: C4023721
Disease: Abnormal hair pattern
Abnormal hair pattern
15 0 1 6.7E-02 0 0
CUI: C0011981
Disease: Diaphragmatic Eventration
Diaphragmatic Eventration
16 0 1 6.2E-02 0 0
CUI: C1321884
Disease: Atresia of vagina
Atresia of vagina
16 0 1 6.2E-02 0 0
CUI: C4025329
Disease: Abnormality of the anus
Abnormality of the anus
16 1 1 6.2E-02 1 1.00
CUI: C0238441
Disease: Subglottic stenosis
Subglottic stenosis
17 0 1 5.9E-02 0 0
CUI: C1861921
Disease: Cutaneous syndactyly
Cutaneous syndactyly
17 0 1 5.9E-02 0 0
CUI: C0152233
Disease: Congenital ankyloblepharon
Congenital ankyloblepharon
18 0 1 5.6E-02 0 0
CUI: C0339182
Disease: Ankyloblepharon
Ankyloblepharon
18 0 1 5.6E-02 0 0