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: 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
CUI: C2750234
Disease: Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 		1 0 1 4.3E-02 0 0
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		1 0 1 4.3E-02 0 0
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 		1 0 1 4.3E-02 0 0
CUI: C4011726
Disease: MYOPATHY, TUBULAR AGGREGATE, 1
MYOPATHY, TUBULAR AGGREGATE, 1 		1 0 1 4.3E-02 0 0
CUI: C4021006
Disease: Short distal phalanx of the 5th toe
Short distal phalanx of the 5th toe 		1 0 1 4.3E-02 0 0
CUI: C4021280
Disease: Curved 4th toe phalanx
Curved 4th toe phalanx 		1 0 1 4.3E-02 0 0
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia 		1 0 1 4.3E-02 0 0