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: C0020538
Disease: Hypertensive disease
Hypertensive disease
2322 1085 137 5.7E-02 4 3.6E-03
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
2803 824 120 4.1E-02 1 1.2E-03
CUI: C0011847
Disease: Diabetes
Diabetes
2359 710 97 3.9E-02 1 1.4E-03
CUI: C4746986
Disease: ALPORT SYNDROME 1, X-LINKED
ALPORT SYNDROME 1, X-LINKED
2 450 1 4.2E-03 1 2.1E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 337 41 4.4E-02 4 1.1E-02
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome
51 314 20 7.4E-02 1 3.0E-03
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
666 194 95 0.12 1 4.7E-03
Finnish congenital nephrotic syndrome
11 178 3 1.2E-02 1 5.1E-03
CUI: C0027092
Disease: Myopia
Myopia
490 167 35 5.0E-02 2 1.1E-02
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
4 143 4 1.7E-02 1 6.2E-03
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
1180 140 128 9.9E-02 1 6.3E-03
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
440 139 44 6.9E-02 1 6.3E-03
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
405 135 38 6.3E-02 1 6.5E-03
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
82 132 3 9.4E-03 2 1.3E-02
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder)
64 116 2 6.6E-03 1 7.4E-03
Sensorineural Hearing Loss (disorder)
783 111 76 8.0E-02 1 7.7E-03
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
592 110 59 7.6E-02 1 7.8E-03
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
51 72 11 3.9E-02 2 2.2E-02
CUI: C0011991
Disease: Diarrhea
Diarrhea
632 63 44 5.3E-02 1 1.2E-02
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
31 53 21 8.4E-02 2 2.8E-02
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis
281 50 63 0.14 2 2.9E-02
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure
391 49 11 1.8E-02 1 1.5E-02
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
384 45 110 0.21 2 3.2E-02
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
3 43 3 1.3E-02 1 1.6E-02
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
615 42 120 0.16 1 1.6E-02