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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: Hyperlipidemias (D006949)
..Starting node ..Hyperlipoproteinemias (D006951)
Child Nodes:
........Apolipoprotein C-III Deficiency (C566270)
........Chylomicronemia, Familial, due to Circulating Inhibitor of Lipoprotein Lipase (C566126)
........HYPERALPHALIPOPROTEINEMIA 1 (OMIM:143470)
........Hypercholesterolemia, Autosomal Dominant, 3 (C566337)
........Hyperlipoproteinemia Type I (D008072) 1
........Hyperlipoproteinemia Type II (D006938) 4
........Hyperlipoproteinemia Type III (D006952)
........Hyperlipoproteinemia Type IV (D006953)
........Hyperlipoproteinemia Type V (D006954)
........Hyperlipoproteinemia, Type II, and Deafness (C564170)
........Lipoprotein Types--Lp System Lp(A) Hyperlipoproteinemia (C563617)
Sister Nodes:
..Hypercholesterolemia (D006937) 5
..Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis (C566263)
..Hyperlipidemia, Familial Combined (D006950) 2
..Hyperlipoproteinemias (D006951) 16
..Hypertriglyceridemia (D015228) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5412
Name:	Hyperlipoproteinemias
Definition:	Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation.
Alternative IDs:
ParentIDs:	MESH:D006949
TreeNumbers:	C18.452.584.500.500.644
Synonyms:	Hyperlipoproteinemia
Slim Mappings:	Metabolic disease
Reference:	MedGen: D006951 MeSH: D006951 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants