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: C0003892
Disease: Neurogenic arthropathy
Neurogenic arthropathy
7 0 4 0.36 0 0
CUI: C0432292
Disease: Familial expansile osteolysis
Familial expansile osteolysis
5 0 3 0.30 0 0
CUI: C0392519
Disease: Calcium deficiency
Calcium deficiency
2 0 2 0.25 0 0
CUI: C1306839
Disease: Pyrophosphate arthritis
Pyrophosphate arthritis
2 0 2 0.25 0 0
Osteopetrosis, mild autosomal recessive form
2 0 2 0.25 0 0
CUI: C0334569
Disease: Odontogenic myxoma
Odontogenic myxoma
8 0 3 0.23 0 0
CUI: C1290638
Disease: Resorption of apex of tooth root
Resorption of apex of tooth root
8 0 3 0.23 0 0
CUI: C1832451
Disease: Cranial hyperostosis
Cranial hyperostosis
10 0 3 0.20 0 0
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome
13 0 3 0.17 0 0
CUI: C4272579
Disease: Autosomal Dominant Osteopetrosis
Autosomal Dominant Osteopetrosis
14 0 3 0.16 0 0
CUI: C0039106
Disease: Pigmented villonodular synovitis
Pigmented villonodular synovitis
15 0 3 0.15 0 0
CUI: C0271344
Disease: Compression of optic nerve
Compression of optic nerve
8 0 2 0.14 0 0
CUI: C0948585
Disease: Hydroxyprolinuria
Hydroxyprolinuria
8 0 2 0.14 0 0
CUI: C0005974
Disease: Bone Resorption
Bone Resorption
10 0 2 0.12 0 0
CUI: C0012767
Disease: Tooth eruption disorder
Tooth eruption disorder
1 0 1 0.12 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy
10 0 2 0.12 0 0
CUI: C0266284
Disease: Lingual Thyroid
Lingual Thyroid
1 0 1 0.12 0 0
CUI: C0334689
Disease: C cell tumor
C cell tumor
1 0 1 0.12 0 0
CUI: C0796418
Disease: Visual Pathway Glioma
Visual Pathway Glioma
10 0 2 0.12 0 0
CUI: C1262008
Disease: Hyperphosphatasemia
Hyperphosphatasemia
1 0 1 0.12 0 0
Mixed medullary-follicular carcinoma
1 0 1 0.12 0 0
Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation
1 0 1 0.12 0 0
CUI: C1608983
Disease: Mal de debarquement
Mal de debarquement
1 0 1 0.12 0 0
CUI: C1709166
Disease: Neoplastic C-Cell Hyperplasia
Neoplastic C-Cell Hyperplasia
1 0 1 0.12 0 0
CUI: C2349460
Disease: Pure menstrual migraine
Pure menstrual migraine
1 0 1 0.12 0 0