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The way concept relations are shown:
Hypobetalipoproteinemia, Familial, Apolipoprotein B
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypobetalipoproteinemia, Familial, Apolipoprotein B 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypobetalipoproteinemia, Familial, Apolipoprotein B 1 coordinate concept∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypobetalipoproteinemia, Familial, Apolipoprotein B 1 coordinate conceptX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypobetalipoproteinemia, Familial, Apolipoprotein B ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypobetalipoproteinemia, Familial, Apolipoprotein B ∟ ∟ ∟ ∟ ∟ ∟ ∟ Hypobetalipoproteinemia, Familial, Apolipoprotein B |
History note: | Apolipoproteins B (1986-2006)X |
historyNote*: | 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE use ABETALIPOPROTEINEMIA 2000-2006
X |
publicMeSHNote*: | 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE see ABETALIPOPROTEINEMIA 2000-2006
X |
Scope note: | An autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 2006-07-05X |
dateEstablished*: | 2007-01-01X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | lktX |
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Labels and equivalent concepts: | Suvuittainen apolipoproteiini B -hypobeetalipoproteinemia (fi) XHypobetalipoproteinemia, Familial, Apo B (en, replaced) Apolipoprotein B Deficiency Disease (en, replaced) Apolipoprotein B Deficiency (en, replaced) Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type (en, replaced) |
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