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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Calcium Metabolism Disorders (D002128)
Parent Node: Water-Electrolyte Imbalance (D014883)
..Starting node ..Hypercalcemia (D006934)
Child Nodes:
........Blue diaper syndrome (C536239)
........Familial benign hypercalcemia, type 3 (C537147)
........Humoral Hypercalcemia Of Malignancy (C562390)
........Hypercalcemia, Idiopathic, of Infancy (C562581)
........Hypercalcemia, Infantile (C562999)
........Hypercalciuric Hypercalcemia (C563373)
........Hypocalciuric Hypercalcemia, Acquired (C564151)
........Hypocalciuric hypercalcemia, familial, type 1 (C537145)
........Hypocalciuric hypercalcemia, familial, type 2 (C537146)
........SHORT syndrome (C537327)
Sister Nodes:
..Dehydration (D003681)
..Hypercalcemia (D006934) 10
..Hyperkalemia (D006947) 4
..Hypernatremia (D006955)
..Hypocalcemia (D006996) 5
..Hypokalemia (D007008) 1
..Hyponatremia (D007010) 1
..Inappropriate ADH Syndrome (D007177) 1
..Water Intoxication (D014869)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5346
Name:	Hypercalcemia
Definition:	Abnormally high level of calcium in the blood.
Alternative IDs:
ParentIDs:	MESH:D002128\|MESH:D014883
TreeNumbers:	C18.452.174.451 \|C18.452.950.340
Synonyms:	Hypercalcemias \|Milk Alkali Syndrome \|Milk-Alkali Syndrome \|Syndrome, Milk-Alkali
Slim Mappings:	Metabolic disease
Reference:	MedGen: D006934 MeSH: D006934 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants