MSeqDR Mitochondrial Disease Portal


 
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Disease Browser
Parent Node:
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Metabolic Diseases (D008659)
..Starting node
..expand
Iron Metabolism Disorders (D019189)

       Child Nodes:
........expandAnemia, Iron-Deficiency (D018798) Child1
........expandFamilial apoceruloplasmin deficiency (C536004)
........expandHeme Oxygenase 1 Deficiency (C564200)
........expandHyperferritinemia, hereditary, with congenital cataracts (C538137)
........expandIron Overload (D019190) Child12  LSDB C:1
........expandNBIA2B (C565699)
........expandNeurodegeneration with brain iron accumulation (NBIA) (C538421) Child2
........expandNeuroferritinopathy (C548080)



 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:5912
Name:Iron Metabolism Disorders
Definition:Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (From Mosby's Medical, Nursing, & Allied Health Dictionary, 4th ed)
Alternative IDs:
ParentIDs:MESH:D008659
TreeNumbers:C18.452.565
Synonyms:Disorder, Iron Metabolism |Disorders, Iron Metabolism |Iron Metabolism Disorder |Metabolism Disorder, Iron |Metabolism Disorders, Iron
Slim Mappings:Metabolic disease
Reference: MedGen: D019189
MeSH: D019189
OMIM:
MSeqDR LSDB:
MSeqDR has 1 matches in descendants: 00104;  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal