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: C0015624
Disease: Fanconi Syndrome
Fanconi Syndrome
26 4 1 3.7E-02 1 6.2E-02
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
26 0 1 3.7E-02 0 0
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
26 0 1 3.7E-02 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa
29 0 1 3.3E-02 0 0
CUI: C1704375
Disease: Hypophosphatemic Rickets
Hypophosphatemic Rickets
29 0 1 3.3E-02 0 0
CUI: C0341703
Disease: Adult Fanconi syndrome
Adult Fanconi syndrome
32 0 1 3.0E-02 0 0
CUI: C4316899
Disease: Cystinosis
Cystinosis
32 27 1 3.0E-02 7 0.21
Progressive neurologic deterioration
33 0 1 2.9E-02 0 0
CUI: C1849039
Disease: Metaphyseal widening
Metaphyseal widening
43 0 1 2.3E-02 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality
49 0 1 2.0E-02 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
50 0 1 2.0E-02 0 0
CUI: C0282201
Disease: Phosphate Diabetes
Phosphate Diabetes
51 0 1 1.9E-02 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria
53 0 1 1.9E-02 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
55 0 1 1.8E-02 0 0
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder
57 0 1 1.7E-02 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia
61 0 1 1.6E-02 0 0
CUI: C0085602
Disease: Polydipsia
Polydipsia
61 0 1 1.6E-02 0 0
CUI: C0151747
Disease: Renal tubular disorder
Renal tubular disorder
64 0 1 1.5E-02 0 0
CUI: C0238621
Disease: Aminoaciduria
Aminoaciduria
68 0 1 1.4E-02 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis
69 0 1 1.4E-02 0 0
CUI: C0085682
Disease: Hypophosphatemia
Hypophosphatemia
69 0 1 1.4E-02 0 0
CUI: C0035579
Disease: Rickets
Rickets
72 0 1 1.4E-02 0 0
CUI: C0085293
Disease: Hepatitis E
Hepatitis E
72 0 1 1.4E-02 0 0
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis
72 0 1 1.4E-02 0 0
CUI: C0032617
Disease: Polyuria
Polyuria
73 0 1 1.4E-02 0 0