1 / 1 DeCS    
Descriptor English:   Hypoalphalipoproteinemias 
Descriptor Spanish:   Hipoalfalipoproteinemias 
Descriptor Portuguese:   Hipoalfalipoproteinemias 
Synonyms English:   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  
Tree Number:   C16.320.565.398.500.330
C18.452.584.500.875.330
C18.452.648.398.500.330
Definition English:   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. 
History Note English:   2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL use TANGIER DISEASE 1995-2006 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   52145 
Unique Identifier:   D052456 


   DISEASES [C]
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
         Genetic Diseases, Inborn [C16.320]
            Metabolism, Inborn Errors [C16.320.565]
               Lipid Metabolism, Inborn Errors [C16.320.565.398]
                  Hypolipoproteinemias [C16.320.565.398.500]
                     Hypoalphalipoproteinemias [C16.320.565.398.500.330] 
                        Lecithin Cholesterol Acyltransferase Deficiency [C16.320.565.398.500.330.500]
                        Tangier Disease [C16.320.565.398.500.330.750]
                     Hypobetalipoproteinemias [C16.320.565.398.500.440] +


   DISEASES [C]
      Nutritional and Metabolic Diseases [C18]
         Metabolic Diseases [C18.452]
            Lipid Metabolism Disorders [C18.452.584]
               Dyslipidemias [C18.452.584.500]
                  Hypolipoproteinemias [C18.452.584.500.875]
                     Hypoalphalipoproteinemias [C18.452.584.500.875.330] 
                        Lecithin Cholesterol Acyltransferase Deficiency [C18.452.584.500.875.330.500]
                        Tangier Disease [C18.452.584.500.875.330.750]
                     Hypobetalipoproteinemias [C18.452.584.500.875.440] +


   DISEASES [C]
      Nutritional and Metabolic Diseases [C18]
         Metabolic Diseases [C18.452]
            Metabolism, Inborn Errors [C18.452.648]
               Lipid Metabolism, Inborn Errors [C18.452.648.398]
                  Hypolipoproteinemias [C18.452.648.398.500]
                     Hypoalphalipoproteinemias [C18.452.648.398.500.330] 
                        Lecithin Cholesterol Acyltransferase Deficiency [C18.452.648.398.500.330.500]
                        Tangier Disease [C18.452.648.398.500.330.750]
                     Hypobetalipoproteinemias [C18.452.648.398.500.440] +