MSeqDR Mitochondrial Disease Portal


 
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Disease Browser
Parent Node:
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Metabolic Diseases (D008659)
..Starting node
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Calcium Metabolism Disorders (D002128)

       Child Nodes:
........expandCalcinosis (D002114) Child50
........expandDecalcification, Pathologic (D003649) Child1
........expandHypercalcemia (D006934) Child10
........expandHypocalcemia (D006996) Child5
........expandHypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475)
........expandMeier Blumberg Imahorn syndrome (C536148)
........expandPseudohypoparathyroidism (D011547) Child6
........expandRickets (D012279) Child16



 Sister Nodes: 
..expandAcid-Base Imbalance (D000137) Child42  LSDB C:10
..expandADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 (OMIM:606770)
..expandADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 (OMIM:606771)
..expandBrain Diseases, Metabolic (D001928) Child244  LSDB C:29
..expandCalcium Metabolism Disorders (D002128) Child94
..expandDNA Repair-Deficiency Disorders (D049914) Child95  LSDB C:1
..expandGlucose Metabolism Disorders (D044882) Child137  LSDB C:6
..expandHyperlactatemia (D065906)
..expandHypermanganesemia with Dystonia Polycythemia and Cirrhosis (C548016)
..expandIron Metabolism Disorders (D019189) Child23  LSDB C:1
..expandLipid Metabolism Disorders (D052439) Child189  LSDB C:9
..expandMalabsorption Syndromes (D008286) Child29
..expandMetabolic Syndrome X (D024821) Child1
..expandMetabolism, Inborn Errors (D008661) Child886  LSDB C:47
..expandMitochondrial Diseases (D028361) Child114  LSDB C:68
..expandPhosphorus Metabolism Disorders (D010760) Child25
..expandPorphyrias (D011164) Child18
..expandProteostasis Deficiencies (D057165) Child55
..expandSHORT syndrome (C537327)
..expandSkin Diseases, Metabolic (D012875) Child33
..expandWasting Syndrome (D019282) Child1
..expandWater-Electrolyte Imbalance (D014883) Child31
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, 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:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal