Source: INFERRED ×
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: C0428302
Disease: Calcium level result
Calcium level result 		14 51 14 0.61 51 0.72
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity 		10 0 2 6.5E-02 0 0
CUI: C0451641
Disease: Urolithiasis
Urolithiasis 		12 17 2 6.1E-02 1 1.1E-02
CUI: C0344539
Disease: Hypoplasia of iris
Hypoplasia of iris 		16 0 2 5.4E-02 0 0
CUI: C1853377
Disease: Enlarged cisterna magna
Enlarged cisterna magna 		18 0 2 5.1E-02 0 0
CUI: C4023681
Disease: Delayed fine motor development
Delayed fine motor development 		19 0 2 5.0E-02 0 0
CUI: C1834536
Disease: Weakness of the intrinsic hand muscles
Weakness of the intrinsic hand muscles 		21 0 2 4.8E-02 0 0
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders 		1 0 1 4.3E-02 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 0 1 4.3E-02 0 0
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		1 0 1 4.3E-02 0 0
CUI: C0342345
Disease: Hypoparathyroidism - autosomal dominant
Hypoparathyroidism - autosomal dominant 		1 0 1 4.3E-02 0 0
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
Hypocalciuric hypercalcemia, familial, type 1 		1 0 1 4.3E-02 0 0
CUI: C0410207
Disease: Tubular Aggregate Myopathy
Tubular Aggregate Myopathy 		1 0 1 4.3E-02 0 0
CUI: C0431401
Disease: Gillespie syndrome
Gillespie syndrome 		1 0 1 4.3E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 4.3E-02 0 0
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia 		1 0 1 4.3E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 4.3E-02 0 0
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
HYPERPARATHYROIDISM, NEONATAL SEVERE 		1 0 1 4.3E-02 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15 		1 0 1 4.3E-02 0 0
CUI: C1850792
Disease: Congenital myasthenic syndrome ib
Congenital myasthenic syndrome ib 		1 0 1 4.3E-02 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism 		1 0 1 4.3E-02 0 0
CUI: C1857787
Disease: Aplasia of the inferior half of the cerebellar vermis
Aplasia of the inferior half of the cerebellar vermis 		1 0 1 4.3E-02 0 0
CUI: C1861451
Disease: Stormorken Syndrome
Stormorken Syndrome 		1 0 1 4.3E-02 0 0
CUI: C1861732
Disease: SPINOCEREBELLAR ATAXIA 29
SPINOCEREBELLAR ATAXIA 29 		1 0 1 4.3E-02 0 0
CUI: C2748557
Disease: Immune dysfunction with T-cell inactivation due to calcium entry defect 2
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 		1 0 1 4.3E-02 0 0