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: C1446648
Disease: Non-specific brain syndrome
Non-specific brain syndrome
1 1 1 0.17 1 0.17
Renal tubular acidosis, distal, type 3
1 0 1 0.17 0 0
CUI: C4017251
Disease: CARBONIC ANHYDRASE II VARIANT
CARBONIC ANHYDRASE II VARIANT
1 0 1 0.17 0 0
CUI: C4272578
Disease: Autosomal Recessive Osteopetrosis
Autosomal Recessive Osteopetrosis
24 0 4 0.15 0 0
CUI: C0342639
Disease: Familial idiopathic hypercalciuria
Familial idiopathic hypercalciuria
2 0 1 0.14 0 0
Transient neonatal renal tubular acidosis
2 0 1 0.14 0 0
CUI: C2673441
Disease: Renal calcium wasting
Renal calcium wasting
3 0 1 0.12 0 0
CUI: C1839866
Disease: Elevated serum acid phosphatase
Elevated serum acid phosphatase
4 0 1 0.11 0 0
CUI: C4531013
Disease: Light induced retinopathy
Light induced retinopathy
5 0 1 1.0E-01 0 0
CUI: C0014647
Disease: Giant Cell Epulis
Giant Cell Epulis
6 0 1 9.1E-02 0 0
CUI: C0155550
Disease: Neural hearing loss
Neural hearing loss
6 0 1 9.1E-02 0 0
CUI: C4551853
Disease: Diaphyseal sclerosis
Diaphyseal sclerosis
6 0 1 9.1E-02 0 0
CUI: C0231779
Disease: Heel toe gait
Heel toe gait
7 0 1 8.3E-02 0 0
CUI: C0271344
Disease: Compression of optic nerve
Compression of optic nerve
8 0 1 7.7E-02 0 0
Peroxisome Biogenesis Disorder, Complementation Group C
8 0 1 7.7E-02 0 0
Rigor - Temperature-associated observation
24 0 2 7.1E-02 0 0
CUI: C4021553
Disease: Periodic hypokalemic paresis
Periodic hypokalemic paresis
9 0 1 7.1E-02 0 0
CUI: C0747742
Disease: polyp benign
polyp benign
10 0 1 6.7E-02 0 0
CUI: C1832451
Disease: Cranial hyperostosis
Cranial hyperostosis
10 0 1 6.7E-02 0 0
CUI: C0162375
Disease: Granuloma, Giant Cell Reparative
Granuloma, Giant Cell Reparative
11 0 1 6.2E-02 0 0
CUI: C0546983
Disease: Post-Concussion Syndrome
Post-Concussion Syndrome
11 0 1 6.2E-02 0 0
CUI: C0005944
Disease: Metabolic Bone Disorder
Metabolic Bone Disorder
66 1 4 5.9E-02 1 0.17
Extramedullary Hematopoiesis Function
16 0 1 4.8E-02 0 0
CUI: C3671887
Disease: Hypernatriuria
Hypernatriuria
17 0 1 4.5E-02 0 0
CUI: C0039147
Disease: Syrinx formation
Syrinx formation
18 0 1 4.3E-02 0 0