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: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
96 8 44 0.18 2 6.9E-02
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney
69 0 37 0.17 0 0
CUI: C4551858
Disease: Vesicoureteral Reflux 1
Vesicoureteral Reflux 1
47 10 32 0.16 3 1.0E-01
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 51 0.14 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine
77 5 32 0.14 1 3.7E-02
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
253 18 51 0.13 2 5.1E-02
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion
211 25 45 0.13 1 2.1E-02
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
237 21 45 0.12 2 4.8E-02
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology
41 0 24 0.12 0 0
Autosomal Recessive Primary Microcephaly
33 0 23 0.12 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
384 96 59 0.12 1 8.5E-03
CUI: C1849172
Disease: Frontal lobe hypoplasia
Frontal lobe hypoplasia
30 0 22 0.11 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts
46 0 23 0.11 0 0
CUI: C0266491
Disease: Neuronal heterotopia
Neuronal heterotopia
67 0 25 0.11 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
284 39 46 0.11 1 1.6E-02
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
225 21 40 0.11 1 2.3E-02
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
235 0 40 0.10 0 0
CUI: C0266383
Disease: Uterine Anomalies
Uterine Anomalies
35 0 21 0.10 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
274 83 43 0.10 1 9.5E-03
CUI: C1865014
Disease: Long philtrum
Long philtrum
282 0 43 0.10 0 0
CUI: C0020545
Disease: Hypertension, Renovascular
Hypertension, Renovascular
78 0 24 1.0E-01 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism
586 0 70 1.0E-01 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
426 0 55 9.9E-02 0 0
CUI: C3553764
Disease: Joint hyperflexibility
Joint hyperflexibility
181 0 33 9.9E-02 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia
104 0 26 9.8E-02 0 0