serw-MX  [xml]  
 


    
 DeCS Categories

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.663 Peroxisomal Disorders .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.663 Peroxisomal Disorders .
F01 Behavior and Behavior Mechanisms .
F01.829 Psychology, Social .
F01.829.263 Family .
F01.829.263.315 Family Characteristics .
F01.829.263.315.500 Marital Status .
F01.829.263.315.500.725 Single Person .
F01.829.263.315.500.725.700 Single Parent .
F01.829.263.500 Nuclear Family .
F01.829.263.500.320 Parents .
F01.829.263.500.320.785 Single Parent .
I01 Social Sciences .
I01.240 Demography .
I01.240.361 Family Characteristics .
I01.240.361.500 Marital Status .
I01.240.361.500.725 Single Person .
I01.240.361.500.725.700 Single Parent .
I01.880 Sociology .
I01.880.853 Sociological Factors .
I01.880.853.150 Family .
I01.880.853.150.423 Family Characteristics .
I01.880.853.150.423.500 Marital Status .
I01.880.853.150.423.500.725 Single Person .
I01.880.853.150.423.500.725.700 Single Parent .
I01.880.853.150.500 Nuclear Family .
I01.880.853.150.500.340 Parents .
I01.880.853.150.500.340.785 Single Parent .
M01 Persons .
M01.620 Parents .
M01.620.785 Single Parent .
M01.785 Single Person .
N01 Population Characteristics .
N01.224 Demography .
N01.224.361 Family Characteristics .
N01.224.361.500 Marital Status .
N01.224.361.500.725 Single Person .
N01.224.361.500.725.700 Single Parent .
N01.824 Socioeconomic Factors .
N01.824.308 Family Characteristics .
N01.824.308.500 Marital Status .
N01.824.308.500.725 Single Person .
N01.824.308.500.725.700 Single Parent .
SP3 Population Studies in Public Health .
SP3.001 Population .
SP3.001.004 Persons .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Single Person .
Maritally Unattached .
Never Married .
Unmarried .
Person, Single .
Persons, Single .
Single Persons .
The unmarried man or woman. .
1.00
192202
 
Persons .
Person .
Named Groups .
Persons as individuals (e.g., ABORTION APPLICANTS) or as members of a group (e.g., HISPANIC AMERICANS). It is not used for members of the various professions (e.g., PHYSICIANS) or occupations (e.g., LIBRARIANS) for which OCCUPATIONAL GROUPS is available. .
0.66
13270
 
Single Parent .
Single Step-Parent .
Single Stepparent .
Parents, Single .
Single Parents .
Single Step Parent .
Single Step-Parents .
Single Stepparents .
Step-Parent, Single .
Step-Parents, Single .
Stepparent, Single .
Stepparents, Single .
Parent, Single .
A natural, adoptive, or substitute parent of a dependent child, who lives with only one parent. The single parent may live with or visit the child. The concept includes the never-married, as well as the divorced and widowed. .
0.60
211126
 
Peroxisomal Disorders .
Adrenoleukodystrophy, Autosomal Neonatal Form .
Adrenoleukodystrophy, Autosomal, Neonatal Form .
Hyperpipecolatemia .
Neonatal Adrenoleukodystrophy .
Peroxisomal Dysfunction, General .
Peroxisomal Dysfunction, Multiple .
Peroxisomal Dysfunction, Single .
Acidemia, Hyperpipecolic .
Acidemias, Hyperpipecolic .
Adrenoleukodystrophies, Neonatal .
Dysfunction, General Peroxisomal .
Dysfunction, Multiple Peroxisomal .
Dysfunction, Single Peroxisomal .
Dysfunctions, General Peroxisomal .
Dysfunctions, Multiple Peroxisomal .
Dysfunctions, Single Peroxisomal .
General Peroxisomal Dysfunction .
General Peroxisomal Dysfunctions .
Hyperpipecolic Acidemias .
Multiple Peroxisomal Dysfunction .
Multiple Peroxisomal Dysfunctions .
Neonatal Adrenoleukodystrophies .
Peroxisomal Disorder .
Peroxisomal Dysfunctions, General .
Peroxisomal Dysfunctions, Multiple .
Peroxisomal Dysfunctions, Single .
Single Peroxisomal Dysfunction .
Single Peroxisomal Dysfunctions .
Adrenoleukodystrophy, Neonatal .
Hyperpipecolic Acidemia .
A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders. .
0.53
7527