Fenilcetonuria Materna

Preferred Label : Fenilcetonuria Materna;

DeCS synonym : Embarazo en Fenilcetonuria; Enfermedad por Deficiencia Materna de Fenilalanina Hidroxilasa;

Details

Origin ID

D017042;

UMLS CUI

C0085547;

Manual NTBT mappings (CISMeF)
- Enfermedad del metabolismo de la fenilalanina o tirosina [ORDO Disease]
- Síndrome de Pierre Robin teratogénico [ORDO Disease]
See also
- Fenilalanina Hidroxilasa [MeSH Descriptor]
UMLS correspondences (same concept)
- Fenilcetonuria materna [ORDO Disease]
- fenilcetonuria materna (trastorno) [Concepto SNOMED CT]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients