| Descriptor English: | Hypoalphalipoproteinemias | ||||||
| Descriptor Spanish: |
Hipoalfalipoproteinemias
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| Descriptor Portuguese: | Hipoalfalipoproteinemias | ||||||
| Descriptor French: | Hypoalphalipoprotéinémies | ||||||
| Entry term(s): |
Familial High Density Lipoprotein Deficiency Disease Familial High-Density Lipoprotein Deficiency Disease Familial Hypoalphalipoproteinemia Familial Hypoalphalipoproteinemias Familial alpha Lipoprotein Deficiency Disease Familial alpha-Lipoprotein Deficiency Disease HDL Cholesterol, Low Serum HDL Lipoprotein Deficiency Disease High Density Lipoprotein Deficiency Disease, Familial High-Density Lipoprotein Deficiency Disease, Familial Hypo alpha Lipoproteinemia Hypo alpha Lipoproteinemias Hypoalphalipoproteinemia Hypoalphalipoproteinemia, Familial Hypoalphalipoproteinemia, Primary Hypoalphalipoproteinemias, Familial Hypoalphalipoproteinemias, Primary Lipoprotein Deficiency Disease, HDL, Familial Lipoproteinemia, Hypo alpha Lipoproteinemias, Hypo alpha Primary Hypoalphalipoproteinemias alpha Lipoprotein Deficiency Disease, Familial alpha Lipoproteinemia, Hypo alpha-Lipoprotein Deficiency Disease, Familial |
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| Tree number(s): |
C16.320.565.398.500.330 C18.452.584.500.875.330 C18.452.584.563.500.330 C18.452.648.398.500.330 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D052456 | ||||||
| Scope note: | Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS. |
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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: |
Lipoproteins, HDL (1981-2006) |
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| Public MeSH Note: | 2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL see TANGIER DISEASE 1995-2006 |
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| History Note: | 2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL use TANGIER DISEASE 1995-2006 |
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| DeCS ID: | 52145 | ||||||
| Unique ID: | D052456 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2007/01/01 | ||||||
| Date of Entry: | 2006/07/05 | ||||||
| Revision Date: | 2013/07/08 |
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Hypoalphalipoproteinemias
- Preferred
Hypoalphalipoproteinemia, Familial
- Narrower
| Concept UI |
M0487118 |
| Scope note | Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS. |
| Preferred term | Hypoalphalipoproteinemias |
| Entry term(s) |
HDL Cholesterol, Low Serum Hypo alpha Lipoproteinemia Hypo alpha Lipoproteinemias Hypoalphalipoproteinemia Lipoproteinemia, Hypo alpha Lipoproteinemias, Hypo alpha alpha Lipoproteinemia, Hypo |
| Concept UI |
M0487126 |
| Preferred term | Hypoalphalipoproteinemia, Familial |
| Entry term(s) |
Familial High Density Lipoprotein Deficiency Disease Familial High-Density Lipoprotein Deficiency Disease Familial Hypoalphalipoproteinemia Familial Hypoalphalipoproteinemias Familial alpha Lipoprotein Deficiency Disease Familial alpha-Lipoprotein Deficiency Disease HDL Lipoprotein Deficiency Disease High Density Lipoprotein Deficiency Disease, Familial High-Density Lipoprotein Deficiency Disease, Familial Hypoalphalipoproteinemia, Primary Hypoalphalipoproteinemias, Familial Hypoalphalipoproteinemias, Primary Lipoprotein Deficiency Disease, HDL, Familial Primary Hypoalphalipoproteinemias alpha Lipoprotein Deficiency Disease, Familial alpha-Lipoprotein Deficiency Disease, Familial |
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