| Descriptor English: | Hyperlipoproteinemia Type III | ||||||
| Descriptor Spanish: |
Hiperlipoproteinemia Tipo III
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| Descriptor Portuguese: | Hiperlipoproteinemia Tipo III | ||||||
| Descriptor French: | Hyperlipoprotéinémie de type III | ||||||
| Entry term(s): |
Autosomal Recessive Hypercholesterolemia Autosomal Recessive Hypercholesterolemias Broad Beta Disease Broad-beta Hyperlipoproteinemia Dysbetalipoproteinemia Dysbetalipoproteinemia, Familial Familial Dysbetalipoproteinemia Familial Hypercholesterolemia with Hyperlipemia Hypercholesterolemia, Autosomal Recessive Hyperlipoproteinemia, Broad beta Hyperlipoproteinemia, Broad-beta Hyperlipoproteinemia, Type III Hyperlipoproteinemias, Type III Recessive Hypercholesterolemia, Autosomal Type III Hyperlipoproteinemia Type III Hyperlipoproteinemias |
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| Tree number(s): |
C16.320.565.398.483 C18.452.584.500.500.644.485 C18.452.584.563.483 C18.452.648.398.483 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006952 | ||||||
| Scope note: | An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Hyperlipidemia/familial & genetic (1966-1979) |
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| Public MeSH Note: | 80 |
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| History Note: | 80 |
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| DeCS ID: | 7133 | ||||||
| Unique ID: | D006952 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1980/01/01 | ||||||
| Date of Entry: | 1979/04/23 | ||||||
| Revision Date: | 2022/04/13 |
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Hyperlipoproteinemia Type III
- Preferred
Autosomal Recessive Hypercholesterolemia
- Related but not broader or narrower
| Concept UI |
M0010834 |
| Scope note | An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides. |
| Preferred term | Hyperlipoproteinemia Type III |
| Entry term(s) |
Broad Beta Disease Broad-beta Hyperlipoproteinemia Dysbetalipoproteinemia Dysbetalipoproteinemia, Familial Familial Dysbetalipoproteinemia Familial Hypercholesterolemia with Hyperlipemia Hyperlipoproteinemia, Broad beta Hyperlipoproteinemia, Broad-beta Hyperlipoproteinemia, Type III Hyperlipoproteinemias, Type III Type III Hyperlipoproteinemia Type III Hyperlipoproteinemias |
| Concept UI |
M000749425 |
| Preferred term | Autosomal Recessive Hypercholesterolemia |
| Entry term(s) |
Autosomal Recessive Hypercholesterolemias Hypercholesterolemia, Autosomal Recessive Recessive Hypercholesterolemia, Autosomal |
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