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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 ..Lipid Metabolism Disorders (D052439)
Child Nodes:
........D-BIFUNCTIONAL PROTEIN DEFICIENCY (OMIM:261515)
........Dyslipidemias (D050171) 57
........Lipid Metabolism, Inborn Errors (D008052) 135
........Lipidoses (D008064) 71
........Lipodystrophy (D008060) 12
........Lipomatosis (D008068) 11
........Xanthomatosis (D014973) 5
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:	6459
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: Genes:
Phenotypes
Disease Causing ClinVar Variants