Source: ALL
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: C4024757
Disease: Malformed lacrimal duct
Malformed lacrimal duct 		3 0 3 1.00 0 0
CUI: C4551480
Disease: FRASER SYNDROME 1
FRASER SYNDROME 1 		3 0 3 1.00 0 0
CUI: C1844537
Disease: Cleft ala nasi
Cleft ala nasi 		4 0 3 0.75 0 0
CUI: C4025412
Disease: Midline nasal groove
Midline nasal groove 		4 0 3 0.75 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		5 0 3 0.60 0 0
CUI: C1857190
Disease: Wide pubic symphysis
Wide pubic symphysis 		5 0 3 0.60 0 0
CUI: C1855425
Disease: Marles Greenberg Persaud syndrome
Marles Greenberg Persaud syndrome 		3 0 2 0.50 0 0
CUI: C4303547
Disease: BNAR syndrome
BNAR syndrome 		3 0 2 0.50 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 3 0.38 0 0
CUI: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 0.33 0 0
CUI: C0424000
Disease: Feeling suicidal (finding)
Feeling suicidal (finding) 		1 0 1 0.33 0 0
CUI: C1852453
Disease: Cryptophthalmos, Unilateral or Bilateral, Isolated
Cryptophthalmos, Unilateral or Bilateral, Isolated 		1 0 1 0.33 0 0
CUI: C1857455
Disease: Extension of hair growth on temples to lateral eyebrow
Extension of hair growth on temples to lateral eyebrow 		1 0 1 0.33 0 0
CUI: C2315717
Disease: Cryptotia
Cryptotia 		1 0 1 0.33 0 0
CUI: C4024990
Disease: Aplasia/Hypoplasia of the sternum
Aplasia/Hypoplasia of the sternum 		1 0 1 0.33 0 0
CUI: C4305274
Disease: Isolated cryptophthalmos
Isolated cryptophthalmos 		1 0 1 0.33 0 0
CUI: C4540036
Disease: FRASER SYNDROME 2
FRASER SYNDROME 2 		1 0 1 0.33 0 0
CUI: C4540040
Disease: FRASER SYNDROME 3
FRASER SYNDROME 3 		1 0 1 0.33 0 0
CUI: C0238394
Disease: Female Pseudohermaphroditism
Female Pseudohermaphroditism 		10 0 3 0.30 0 0
CUI: C0521622
Disease: Bilateral hydronephrosis
Bilateral hydronephrosis 		6 0 2 0.29 0 0
CUI: C0023075
Disease: Laryngostenosis
Laryngostenosis 		11 0 3 0.27 0 0
CUI: C4025717
Disease: Abnormality of the small intestine
Abnormality of the small intestine 		2 0 1 0.25 0 0
CUI: C2673611
Disease: Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant
Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant 		3 0 1 0.20 0 0
CUI: C2673612
Disease: Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive
Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive 		3 0 1 0.20 0 0
CUI: C4023721
Disease: Abnormal hair pattern
Abnormal hair pattern 		15 0 3 0.20 0 0