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: C0344312
Disease: White forelock
White forelock 		12 0 6 8.7E-02 0 0
CUI: C0266610
Disease: Preauricular dimple
Preauricular dimple 		40 0 8 8.4E-02 0 0
CUI: C0263498
Disease: Premature canities
Premature canities 		33 0 7 7.9E-02 0 0
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		33 0 7 7.9E-02 0 0
CUI: C3266898
Disease: Waardenburg Syndrome
Waardenburg Syndrome 		21 0 6 7.7E-02 0 0
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2 		9 0 5 7.5E-02 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction 		87 0 10 7.1E-02 0 0
CUI: C1281931
Disease: Obstruction of nasolacrimal duct
Obstruction of nasolacrimal duct 		12 0 5 7.1E-02 0 0
CUI: C1848519
Disease: WAARDENBURG SYNDROME, TYPE 4A
WAARDENBURG SYNDROME, TYPE 4A 		12 0 5 7.1E-02 0 0
CUI: C1619700
Disease: RENAL ADYSPLASIA
RENAL ADYSPLASIA 		29 0 6 7.0E-02 0 0
CUI: C0009681
Disease: Anomalous pulmonary artery
Anomalous pulmonary artery 		14 0 5 6.9E-02 0 0
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		16 0 5 6.8E-02 0 0
CUI: C3536714
Disease: Renal dysplasia
Renal dysplasia 		95 0 10 6.8E-02 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 11 6.7E-02 0 0
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis 		17 0 5 6.7E-02 0 0
CUI: C0431890
Disease: Hypoplasia of thumb
Hypoplasia of thumb 		49 0 7 6.7E-02 0 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology 		35 0 6 6.5E-02 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 0 8 6.5E-02 0 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		86 0 9 6.4E-02 0 0
CUI: C1968949
Disease: Cakut
Cakut 		72 0 8 6.3E-02 0 0
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		74 0 8 6.2E-02 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 10 6.1E-02 0 0
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities 		42 0 6 6.1E-02 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine 		77 0 8 6.1E-02 0 0
CUI: C1836737
Disease: White eyebrow
White eyebrow 		7 0 4 6.1E-02 0 0