Source: ALL
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: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders 		5 0 2 7.7E-02 0 0
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome 		13 0 2 5.9E-02 0 0
CUI: C1853377
Disease: Enlarged cisterna magna
Enlarged cisterna magna 		18 0 2 5.1E-02 0 0
CUI: C0344539
Disease: Hypoplasia of iris
Hypoplasia of iris 		19 0 2 5.0E-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: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia 		24 0 2 4.4E-02 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 0 1 4.3E-02 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia 		1 0 1 4.3E-02 0 0
CUI: C0475733
Disease: Idiopathic infantile hypercalcemia - mild form
Idiopathic infantile hypercalcemia - mild form 		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: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease 		1 0 1 4.3E-02 0 0
CUI: C0858233
Disease: Stridor, Congenital
Stridor, Congenital 		1 0 1 4.3E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 4.3E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 4.3E-02 0 0
CUI: C1842797
Disease: Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like 		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: 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: C2752062
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 		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: 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: C4225407
Disease: PEELING SKIN SYNDROME 4
PEELING SKIN SYNDROME 4 		1 0 1 4.3E-02 0 0