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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: Metabolic Diseases (D008659)
..Starting node ..Calcium Metabolism Disorders (D002128)
Child Nodes:
........Calcinosis (D002114) 50
........Decalcification, Pathologic (D003649) 1
........Hypercalcemia (D006934) 10
........Hypocalcemia (D006996) 5
........Hypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475)
........Meier Blumberg Imahorn syndrome (C536148)
........Pseudohypoparathyroidism (D011547) 6
........Rickets (D012279) 16
Sister Nodes:
..Acid-Base Imbalance (D000137) 42
..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 (OMIM:606770)
..ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 (OMIM:606771)
..Brain Diseases, Metabolic (D001928) 244
..Calcium Metabolism Disorders (D002128) 94
..DNA Repair-Deficiency Disorders (D049914) 95
..Glucose Metabolism Disorders (D044882) 137
..Hyperlactatemia (D065906)
..Hypermanganesemia with Dystonia Polycythemia and Cirrhosis (C548016)
..Iron Metabolism Disorders (D019189) 23
..Lipid Metabolism Disorders (D052439) 189
..Malabsorption Syndromes (D008286) 29
..Metabolic Syndrome X (D024821) 1
..Metabolism, Inborn Errors (D008661) 886
..Mitochondrial Diseases (D028361) 114
..Phosphorus Metabolism Disorders (D010760) 25
..Porphyrias (D011164) 18
..Proteostasis Deficiencies (D057165) 55
..SHORT syndrome (C537327)
..Skin Diseases, Metabolic (D012875) 33
..Wasting Syndrome (D019282) 1
..Water-Electrolyte Imbalance (D014883) 31
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1572
Name:	Calcium Metabolism Disorders
Definition:	Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization.
Alternative IDs:
ParentIDs:	MESH:D008659
TreeNumbers:	C18.452.174
Synonyms:	Calcium Metabolism Disorder \|Disorder, Calcium Metabolism \|Disorders, Calcium Metabolism
Slim Mappings:	Metabolic disease
Reference:	MedGen: D002128 MeSH: D002128 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants