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CIM11 5C50.02

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09

Embryofetopathy due to maternal phenylketonuria

chapitre
05 Endocrine, nutritional or metabolic diseases
bloc
Inborn errors of metabolism
definition
Maternal phenylalaninaemia refers to developmental anomalies that may occur in offspring of women affected by phenylketonuria (PKU), and include fetal development disorders, including microcephaly, intrauterine growth retardation, and subsequent intellectual deficit, and embryo development disorders
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#1509230254 ↗