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: C1706410
Disease: Atopic IgE-mediated allergic disorder
Atopic IgE-mediated allergic disorder 		3 0 1 0.14 0 0
CUI: C1855425
Disease: Marles Greenberg Persaud syndrome
Marles Greenberg Persaud syndrome 		3 0 1 0.14 0 0
CUI: C4024757
Disease: Malformed lacrimal duct
Malformed lacrimal duct 		3 0 1 0.14 0 0
CUI: C4024773
Disease: Lacrimal duct aplasia
Lacrimal duct aplasia 		3 0 1 0.14 0 0
CUI: C4303547
Disease: BNAR syndrome
BNAR syndrome 		3 0 1 0.14 0 0
CUI: C4551480
Disease: FRASER SYNDROME 1
FRASER SYNDROME 1 		3 0 1 0.14 0 0
CUI: C0221215
Disease: Common atrioventricular canal
Common atrioventricular canal 		4 0 1 0.12 0 0
CUI: C0281890
Disease: Laryngeal web
Laryngeal web 		4 0 1 0.12 0 0
CUI: C0342317
Disease: Loss of hypoglycemic warning
Loss of hypoglycemic warning 		4 0 1 0.12 0 0
CUI: C0729198
Disease: Decreased circulating parathyroid hormone level
Decreased circulating parathyroid hormone level 		4 0 1 0.12 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome 		4 0 1 0.12 0 0
CUI: C0877203
Disease: Respiratory tract infection viral
Respiratory tract infection viral 		4 0 1 0.12 0 0
CUI: C1321907
Disease: Congenital absence of parathyroid gland
Congenital absence of parathyroid gland 		4 0 1 0.12 0 0
CUI: C1389851
Disease: Parathyroid hypoplasia
Parathyroid hypoplasia 		4 0 1 0.12 0 0
CUI: C1844537
Disease: Cleft ala nasi
Cleft ala nasi 		4 0 1 0.12 0 0
CUI: C1848670
Disease: Aplasia/Hypoplasia of the phalanges of the hand
Aplasia/Hypoplasia of the phalanges of the hand 		4 0 1 0.12 0 0
CUI: C1851897
Disease: Anterior creases of earlobe
Anterior creases of earlobe 		4 0 1 0.12 0 0
CUI: C1855772
Disease: Absent corpus callosum cataract immunodeficiency
Absent corpus callosum cataract immunodeficiency 		4 0 1 0.12 0 0
CUI: C1865305
Disease: Hypoplastic superior helix
Hypoplastic superior helix 		4 0 1 0.12 0 0
CUI: C2931072
Disease: Epidermolysa bullosa simplex and limb girdle muscular dystrophy
Epidermolysa bullosa simplex and limb girdle muscular dystrophy 		4 0 1 0.12 0 0
CUI: C3150966
Disease: Supernumerary der(22)t(8;22) syndrome
Supernumerary der(22)t(8;22) syndrome 		4 0 1 0.12 0 0
CUI: C4025412
Disease: Midline nasal groove
Midline nasal groove 		4 0 1 0.12 0 0
CUI: C0158629
Disease: Congenital anomaly of aortic arch
Congenital anomaly of aortic arch 		5 0 1 0.11 0 0
CUI: C0264480
Disease: Bakers' asthma
Bakers' asthma 		5 0 1 0.11 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		5 0 1 0.11 0 0