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: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 1.00 0 0
CUI: C4024990
Disease: Aplasia/Hypoplasia of the sternum
Aplasia/Hypoplasia of the sternum 		1 0 1 1.00 0 0
CUI: C4025717
Disease: Abnormality of the small intestine
Abnormality of the small intestine 		2 0 1 0.50 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: C0281890
Disease: Laryngeal web
Laryngeal web 		4 0 1 0.25 0 0
CUI: C1844537
Disease: Cleft ala nasi
Cleft ala nasi 		4 0 1 0.25 0 0
CUI: C1848670
Disease: Aplasia/Hypoplasia of the phalanges of the hand
Aplasia/Hypoplasia of the phalanges of the hand 		4 0 1 0.25 0 0
CUI: C1865305
Disease: Hypoplastic superior helix
Hypoplastic superior helix 		4 0 1 0.25 0 0
CUI: C4025412
Disease: Midline nasal groove
Midline nasal groove 		4 0 1 0.25 0 0
CUI: C0262650
Disease: Abnormality of the thymus
Abnormality of the thymus 		5 0 1 0.20 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		5 0 1 0.20 0 0
CUI: C1857190
Disease: Wide pubic symphysis
Wide pubic symphysis 		5 0 1 0.20 0 0
CUI: C4025208
Disease: Severe T-cell immunodeficiency
Severe T-cell immunodeficiency 		5 0 1 0.20 0 0
CUI: C0521622
Disease: Bilateral hydronephrosis
Bilateral hydronephrosis 		6 0 1 0.17 0 0
CUI: C1857456
Disease: Morphological abnormality of the middle ear
Morphological abnormality of the middle ear 		6 0 1 0.17 0 0
CUI: C1863872
Disease: Coloboma of superior eyelid
Coloboma of superior eyelid 		6 0 1 0.17 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 1 0.12 0 0
CUI: C1853406
Disease: Difficulty in tongue movements
Difficulty in tongue movements 		8 0 1 0.12 0 0
CUI: C0238394
Disease: Female Pseudohermaphroditism
Female Pseudohermaphroditism 		10 0 1 1.0E-01 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 1 1.0E-01 0 0
CUI: C0023075
Disease: Laryngostenosis
Laryngostenosis 		11 0 1 9.1E-02 0 0