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: C0597854
Disease: renin induced hypertension
renin induced hypertension
11 0 9 0.12 0 0
CUI: C0029442
Disease: Osteomalacia
Osteomalacia
31 0 11 0.12 0 0
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
13 0 9 0.12 0 0
Nephrogenic Syndrome of Inappropriate Antidiuresis
14 0 9 0.12 0 0
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism
34 0 11 0.12 0 0
CUI: C0598428
Disease: genetic hypertension
genetic hypertension
34 0 11 0.12 0 0
CUI: C0268079
Disease: Hyperphosphaturia
Hyperphosphaturia
25 0 10 0.11 0 0
CUI: C0342494
Disease: Adrenocortical hyperplasia
Adrenocortical hyperplasia
25 0 10 0.11 0 0
CUI: C4721452
Disease: Intestinal T-Cell Lymphoma
Intestinal T-Cell Lymphoma
35 0 11 0.11 0 0
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
190 71 26 0.11 4 4.8E-02
Enteropathy-Associated T-Cell Lymphoma
39 0 11 0.11 0 0
CUI: C0020438
Disease: Hypercalciuria
Hypercalciuria
60 0 13 0.11 0 0
CUI: C0936282
Disease: Blastoma
Blastoma
20 0 9 0.11 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis
31 0 10 0.11 0 0
Primary Pigmented Nodular Adrenal Dysplasia
31 0 10 0.11 0 0
Hypogonadism, Isolated Hypogonadotropic
42 0 11 0.11 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
94 0 16 0.11 0 0
Primary pigmented nodular adrenocortical disease
22 0 9 0.11 0 0
CUI: C0392525
Disease: Nephrolithiasis
Nephrolithiasis
242 99 30 0.11 4 3.6E-02
CUI: C0085681
Disease: Hyperphosphatemia (disorder)
Hyperphosphatemia (disorder)
65 0 13 0.10 0 0
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma
23 0 9 0.10 0 0
CUI: C3540852
Disease: Rickets, X-Linked Hypophosphatemic
Rickets, X-Linked Hypophosphatemic
23 0 9 0.10 0 0
CUI: C1368019
Disease: Paget Disease
Paget Disease
66 0 13 0.10 0 0
Postural Orthostatic Tachycardia Syndrome
25 0 9 0.10 0 0
CUI: C1837081
Disease: Tibial bowing
Tibial bowing
25 0 9 0.10 0 0