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: C0546969
Disease: Preauricular Fistulae, Congenital
Preauricular Fistulae, Congenital 		4 0 1 0.14 0 0
CUI: C3826233
Disease: Hearing impaired children
Hearing impaired children 		4 0 1 0.14 0 0
CUI: C0265274
Disease: Achondrogenesis, type IB (disorder)
Achondrogenesis, type IB (disorder) 		5 0 1 0.12 0 0
CUI: C0271826
Disease: Iodide transport defect
Iodide transport defect 		5 0 1 0.12 0 0
CUI: C1704380
Disease: Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis 		23 0 3 0.12 0 0
CUI: C1853205
Disease: Glycosylphosphatidylinositol deficiency
Glycosylphosphatidylinositol deficiency 		5 0 1 0.12 0 0
CUI: C0155550
Disease: Neural hearing loss
Neural hearing loss 		6 0 1 0.11 0 0
CUI: C0311237
Disease: Goniodysgenesis
Goniodysgenesis 		6 0 1 0.11 0 0
CUI: C1846348
Disease: Renal potassium wasting
Renal potassium wasting 		6 0 1 0.11 0 0
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome 		6 0 1 0.11 0 0
CUI: C0302859
Disease: Euthyroid Goiter
Euthyroid Goiter 		7 0 1 1.0E-01 0 0
CUI: C0040583
Disease: Tracheal Stenosis
Tracheal Stenosis 		30 0 3 9.7E-02 0 0
CUI: C0342488
Disease: Mineralocorticoid Excess Syndrome, Apparent
Mineralocorticoid Excess Syndrome, Apparent 		8 0 1 9.1E-02 0 0
CUI: C1853666
Disease: Anemia, Diamond-Blackfan, 2
Anemia, Diamond-Blackfan, 2 		8 0 1 9.1E-02 0 0
CUI: C0022681
Disease: Medullary sponge kidney
Medullary sponge kidney 		9 0 1 8.3E-02 0 0
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 0 3 8.3E-02 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss 		22 0 2 8.3E-02 0 0
CUI: C0038478
Disease: Struma Ovarii
Struma Ovarii 		10 0 1 7.7E-02 0 0
CUI: C0085570
Disease: Hypokalemic alkalosis
Hypokalemic alkalosis 		10 0 1 7.7E-02 0 0
CUI: C0240783
Disease: Increased circulating renin level
Increased circulating renin level 		10 0 1 7.7E-02 0 0
CUI: C0392485
Disease: Congenital diverticulum of pharynx
Congenital diverticulum of pharynx 		10 0 1 7.7E-02 0 0
CUI: C0740898
Disease: Hypokalemic metabolic alkalosis
Hypokalemic metabolic alkalosis 		10 0 1 7.7E-02 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 3 7.7E-02 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion 		10 0 1 7.7E-02 0 0
CUI: C0206586
Disease: Endolymphatic Hydrops
Endolymphatic Hydrops 		11 0 1 7.1E-02 0 0