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: C0201925
Disease: Calcium measurement
Calcium measurement 		23 71 14 0.61 51 0.72
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders 		5 0 2 0.12 0 0
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome 		13 0 2 8.0E-02 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 0 1 7.1E-02 0 0
CUI: C0475733
Disease: Idiopathic infantile hypercalcemia - mild form
Idiopathic infantile hypercalcemia - mild form 		1 0 1 7.1E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 7.1E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 7.1E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 7.1E-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 7.1E-02 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism 		1 0 1 7.1E-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 7.1E-02 0 0
CUI: C2752062
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 		1 0 1 7.1E-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 7.1E-02 0 0
CUI: C4021006
Disease: Short distal phalanx of the 5th toe
Short distal phalanx of the 5th toe 		1 0 1 7.1E-02 0 0
CUI: C4225407
Disease: PEELING SKIN SYNDROME 4
PEELING SKIN SYNDROME 4 		1 0 1 7.1E-02 0 0
CUI: C4304527
Disease: 6q25 microdeletion syndrome
6q25 microdeletion syndrome 		1 0 1 7.1E-02 0 0
CUI: C4551629
Disease: Congenital talipes calcaneovalgus
Congenital talipes calcaneovalgus 		1 0 1 7.1E-02 0 0
CUI: C4747885
Disease: HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES
HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES 		1 0 1 7.1E-02 0 0
CUI: C0342639
Disease: Familial idiopathic hypercalciuria
Familial idiopathic hypercalciuria 		2 0 1 6.7E-02 0 0
CUI: C0345406
Disease: Neonatal hyperparathyroidism
Neonatal hyperparathyroidism 		2 0 1 6.7E-02 0 0
CUI: C0853277
Disease: Pseudo-Bartter syndrome
Pseudo-Bartter syndrome 		2 0 1 6.7E-02 0 0
CUI: C0865171
Disease: parathyroiditis
parathyroiditis 		2 0 1 6.7E-02 0 0
CUI: C1857788
Disease: Atrophy of the dentate nucleus
Atrophy of the dentate nucleus 		2 0 1 6.7E-02 0 0
CUI: C3150215
Disease: CHROMOSOME 6q24-q25 DELETION SYNDROME
CHROMOSOME 6q24-q25 DELETION SYNDROME 		2 0 1 6.7E-02 0 0
CUI: C3807541
Disease: MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY 		2 0 1 6.7E-02 0 0