Phenylketonuria, Maternal
"Phenylketonuria, Maternal" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition occurring in untreated or partially treated females with PHENYLKETONURIA when they become pregnant. This may result in damages to the FETUS, including MICROCEPHALY; MENTAL RETARDATION; congenital heart disease; FETAL GROWTH RETARDATION; and CRANIOFACIAL ABNORMALITIES. (From Am J Med Genet 1997 Mar 3;69(1):89-95)
| Descriptor ID |
D017042
|
| MeSH Number(s) |
C10.228.140.163.100.687.500 C13.703.575 C16.320.565.100.766.500 C16.320.565.189.687.500 C18.452.132.100.687.500 C18.452.648.100.766.500 C18.452.648.189.687.500
|
| Concept/Terms |
Phenylketonuria, Maternal- Phenylketonuria, Maternal
- Maternal Phenylketonuria
- Phenylalanine-Hydroxylase Deficiency Disease, Maternal
- Phenylalanine Hydroxylase Deficiency Disease, Maternal
- PKU, Maternal
- Maternal Phenylalanine Hydroxylase Deficiency Disease
- Pregnancy in Phenylketonuria
- Phenylketonuria, Pregnancy in
|
Below are MeSH descriptors whose meaning is more general than "Phenylketonuria, Maternal".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Phenylketonurias [C10.228.140.163.100.687]
- Phenylketonuria, Maternal [C10.228.140.163.100.687.500]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Pregnancy Complications [C13.703]
- Phenylketonuria, Maternal [C13.703.575]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
- Phenylketonurias [C16.320.565.100.766]
- Phenylketonuria, Maternal [C16.320.565.100.766.500]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Phenylketonurias [C16.320.565.189.687]
- Phenylketonuria, Maternal [C16.320.565.189.687.500]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Phenylketonurias [C18.452.132.100.687]
- Phenylketonuria, Maternal [C18.452.132.100.687.500]
- Metabolism, Inborn Errors [C18.452.648]
- Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
- Phenylketonurias [C18.452.648.100.766]
- Phenylketonuria, Maternal [C18.452.648.100.766.500]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Phenylketonurias [C18.452.648.189.687]
- Phenylketonuria, Maternal [C18.452.648.189.687.500]
Below are MeSH descriptors whose meaning is more specific than "Phenylketonuria, Maternal".
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