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: C4272579
Disease: Autosomal Dominant Osteopetrosis
Autosomal Dominant Osteopetrosis
14 0 6 0.19 0 0
CUI: C0262586
Disease: Osteopenia/osteoporosis
Osteopenia/osteoporosis
16 0 5 0.15 0 0
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome
13 0 4 0.12 0 0
Osteoarthropathy, Primary Hypertrophic
14 0 4 0.12 0 0
CUI: C0039106
Disease: Pigmented villonodular synovitis
Pigmented villonodular synovitis
15 0 4 0.12 0 0
CUI: C0035086
Disease: Renal Osteodystrophy
Renal Osteodystrophy
16 0 4 0.11 0 0
CUI: C0003892
Disease: Neurogenic arthropathy
Neurogenic arthropathy
7 0 3 0.11 0 0
Hyperphosphatasemia with bone disease
8 0 3 0.11 0 0
CUI: C1290638
Disease: Resorption of apex of tooth root
Resorption of apex of tooth root
8 0 3 0.11 0 0
CUI: C0085696
Disease: Chronic prostatitis
Chronic prostatitis
20 0 4 0.10 0 0
CUI: C0035851
Disease: Root Resorption
Root Resorption
43 0 6 1.0E-01 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy
10 0 3 1.0E-01 0 0
Hypophosphatemic Rickets, X-Linked Dominant
54 0 7 1.0E-01 0 0
CUI: C1832451
Disease: Cranial hyperostosis
Cranial hyperostosis
10 0 3 1.0E-01 0 0
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
Hyperparathyroidism, Secondary
68 0 8 9.6E-02 0 0
Vitamin D-Resistant Rickets, X-Linked
48 0 6 9.2E-02 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria
13 0 3 9.1E-02 0 0
CUI: C0265224
Disease: Freeman-Sheldon syndrome
Freeman-Sheldon syndrome
26 0 4 8.9E-02 0 0
CUI: C0745106
Disease: hyperparathyroid
hyperparathyroid
14 0 3 8.8E-02 0 0
CUI: C0392519
Disease: Calcium deficiency
Calcium deficiency
2 0 2 8.7E-02 0 0
CUI: C1290009
Disease: Chronic disease of skin
Chronic disease of skin
2 0 2 8.7E-02 0 0
CUI: C1306839
Disease: Pyrophosphate arthritis
Pyrophosphate arthritis
2 0 2 8.7E-02 0 0
CUI: C3839205
Disease: Signet-ring stromal tumor
Signet-ring stromal tumor
2 0 2 8.7E-02 0 0
CUI: C0270948
Disease: Neurogenic Muscular Atrophy
Neurogenic Muscular Atrophy
15 0 3 8.6E-02 0 0
CUI: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome
15 0 3 8.6E-02 0 0