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: C4023397
Disease: Abnormal hair quantity
Abnormal hair quantity 		29 0 10 0.19 0 0
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		11 0 7 0.18 0 0
CUI: C1527404
Disease: Female Pseudo-Turner Syndrome
Female Pseudo-Turner Syndrome 		11 0 7 0.18 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		13 0 7 0.17 0 0
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		23 0 8 0.16 0 0
CUI: C1843181
Disease: Noonan syndrome-like disorder with loose anagen hair
Noonan syndrome-like disorder with loose anagen hair 		19 0 7 0.15 0 0
CUI: C1834124
Disease: Shield chest
Shield chest 		12 0 6 0.15 0 0
CUI: C3501846
Disease: Noonan-Like Syndrome With Loose Anagen Hair
Noonan-Like Syndrome With Loose Anagen Hair 		22 0 7 0.14 0 0
CUI: C0558165
Disease: Curly hair (finding)
Curly hair (finding) 		24 0 7 0.13 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		28 0 7 0.12 0 0
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		11 0 5 0.12 0 0
CUI: C1850171
Disease: Neonatal short-limb short stature
Neonatal short-limb short stature 		12 0 5 0.12 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology 		42 0 8 0.12 0 0
CUI: C1857539
Disease: Deep palmar crease
Deep palmar crease 		23 0 6 0.12 0 0
CUI: C4025662
Disease: Abnormality of the ulna
Abnormality of the ulna 		14 0 5 0.11 0 0
CUI: C1864796
Disease: Pectus excavatum of inferior sternum
Pectus excavatum of inferior sternum 		5 0 4 0.11 0 0
CUI: C4024890
Disease: Excessive wrinkled skin
Excessive wrinkled skin 		25 0 6 0.11 0 0
CUI: C4023385
Disease: Aplasia of the semicircular canal
Aplasia of the semicircular canal 		16 0 5 0.11 0 0
CUI: C4023170
Disease: Abnormal oral mucosa morphology
Abnormal oral mucosa morphology 		6 0 4 0.11 0 0
CUI: C4551484
Disease: Leopard Syndrome 1
Leopard Syndrome 1 		6 0 4 0.11 0 0
CUI: C1837732
Disease: Thickened helices
Thickened helices 		37 0 7 0.11 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation 		59 0 9 0.11 0 0
CUI: C4022755
Disease: Functional abnormality of the gastrointestinal tract
Functional abnormality of the gastrointestinal tract 		7 0 4 0.11 0 0
CUI: C1857002
Disease: Capitate-hamate fusion
Capitate-hamate fusion 		8 0 4 0.10 0 0
CUI: C0014588
Disease: Epispadias
Epispadias 		30 0 6 0.10 0 0