Hyppää sisältöön

Medical Subject Headings

Hae sanastosta

Sisällön kieli

Käsitteen tiedot

Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Pregnancy Complications > Phenylketonuria, Maternal
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Phenylketonurias > Phenylketonuria, Maternal
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Phenylketonurias > Phenylketonuria, Maternal
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Phenylketonurias > Phenylketonuria, Maternal
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Phenylketonurias > Phenylketonuria, Maternal
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Phenylketonurias > Phenylketonuria, Maternal
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Phenylketonurias > Phenylketonuria, Maternal

Käytettävä termi

Phenylketonuria, Maternal  

Tyyppi

  • Topical Descriptor

Yläkäsite

Assosiatiiviset käsitteet

Ohjaustermit

  • Maternal Phenylalanine Hydroxylase Deficiency Disease
  • Maternal Phenylketonuria
  • Phenylalanine Hydroxylase Deficiency Disease, Maternal
  • Phenylalanine-Hydroxylase Deficiency Disease, Maternal
  • Phenylketonuria, Pregnancy in
  • PKU, Maternal
  • Pregnancy in Phenylketonuria

Huomautus

  • check the tags PREGNANCY & FEMALE; consider also PHENYLALANINE HYDROXYLASE /defic

Käyttöhuomautus

  • 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)

Huomautus muutoshistoriasta

  • 1992

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D017042

Lataa tämä käsite:

RDF/XML TURTLE JSON-LD Luotu 30.5.1991, viimeksi muokattu 11.4.2022