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: C1855425
Disease: Marles Greenberg Persaud syndrome
Marles Greenberg Persaud syndrome 		3 0 2 0.29 0 0
CUI: C4024757
Disease: Malformed lacrimal duct
Malformed lacrimal duct 		3 0 2 0.29 0 0
CUI: C4024773
Disease: Lacrimal duct aplasia
Lacrimal duct aplasia 		3 0 2 0.29 0 0
CUI: C4303547
Disease: BNAR syndrome
BNAR syndrome 		3 0 2 0.29 0 0
CUI: C4551480
Disease: FRASER SYNDROME 1
FRASER SYNDROME 1 		3 0 2 0.29 0 0
CUI: C1844537
Disease: Cleft ala nasi
Cleft ala nasi 		4 0 2 0.25 0 0
CUI: C4025412
Disease: Midline nasal groove
Midline nasal groove 		4 0 2 0.25 0 0
CUI: C0022594
Disease: Keratosis Blennorrhagica
Keratosis Blennorrhagica 		5 0 2 0.22 0 0
CUI: C0086501
Disease: Keratoma
Keratoma 		5 0 2 0.22 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		5 0 2 0.22 0 0
CUI: C1857190
Disease: Wide pubic symphysis
Wide pubic symphysis 		5 0 2 0.22 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output 		1 0 1 0.17 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 2 0.17 0 0
CUI: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 0.17 0 0
CUI: C0600177
Disease: Low Cardiac Output Syndrome
Low Cardiac Output Syndrome 		1 0 1 0.17 0 0
CUI: C1852453
Disease: Cryptophthalmos, Unilateral or Bilateral, Isolated
Cryptophthalmos, Unilateral or Bilateral, Isolated 		1 0 1 0.17 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 0.17 0 0
CUI: C2315717
Disease: Cryptotia
Cryptotia 		1 0 1 0.17 0 0
CUI: C4024990
Disease: Aplasia/Hypoplasia of the sternum
Aplasia/Hypoplasia of the sternum 		1 0 1 0.17 0 0
CUI: C4305274
Disease: Isolated cryptophthalmos
Isolated cryptophthalmos 		1 0 1 0.17 0 0
CUI: C4479416
Disease: SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY 		1 0 1 0.17 0 0
CUI: C4540036
Disease: FRASER SYNDROME 2
FRASER SYNDROME 2 		1 0 1 0.17 0 0
CUI: C4540293
Disease: IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA 		1 0 1 0.17 0 0
CUI: C0152014
Disease: Atrophy of pancreas
Atrophy of pancreas 		10 0 2 0.14 0 0
CUI: C0238394
Disease: Female Pseudohermaphroditism
Female Pseudohermaphroditism 		10 0 2 0.14 0 0