MeSH Browser

MeSH Heading: Phenylketonuria, Maternal
Tree Number(s): C10.228.140.163.100.687.500; C12.050.703.575; 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
Unique ID: D017042
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D017042
Annotation: check the tags PREGNANCY & FEMALE; consider also PHENYLALANINE HYDROXYLASE /‌defic
Scope Note: 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)
Entry Version: PKU MATERNAL
Entry Term(s): Maternal Phenylalanine Hydroxylase Deficiency Disease; Maternal Phenylketonuria; PKU, Maternal; Phenylalanine-Hydroxylase Deficiency Disease, Maternal; Pregnancy in Phenylketonuria
Previous Indexing: Phenylketonuria (1966-1991)
See Also: Phenylalanine Hydroxylase
Public MeSH Note: 1992
History Note: 1992
Date Established: 1992/01/01
Date of Entry: 1991/05/30
Revision Date: 2021/06/30

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Phenylketonuria, Maternal MeSH Descriptor Data 2024