MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, UMDF: 1= Disease, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, Myopathy, SANDO
Disease Browser
Parent Node:
expandMetabolic Diseases (D008659)
..Starting node
..expandLipid Metabolism Disorders (D052439)

       Child Nodes:
........expandD-BIFUNCTIONAL PROTEIN DEFICIENCY (OMIM:261515)
........expandDyslipidemias (D050171) Child57
........expandLipid Metabolism, Inborn Errors (D008052) Child135  LSDB C:9
........expandLipidoses (D008064) Child71
........expandLipodystrophy (D008060) Child12
........expandLipomatosis (D008068) Child11
........expandXanthomatosis (D014973) Child5



 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)
..expandBone Diseases, Metabolic (D001851) Child67
..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 (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:7079
Name:Lipid Metabolism Disorders
Definition:Pathological conditions resulting from abnormal anabolism or catabolism of lipids in the body.
Alternative IDs:
ParentIDs:MESH:D008659
TreeNumbers:C18.452.584
Synonyms:Lipid Metabolism Disorder |Metabolism Disorder, Lipid |Metabolism Disorders, Lipid
Slim Mappings:Metabolic disease
Reference: MedGen: D052439
MeSH: D052439
OMIM:
MSeqDR LSDB:
MSeqDR has 9 matches in descendants: 00399; 00417; 00434; 00435; 00436; 00437; 00440; 00466; 00486;  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal