ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2F — Syndromes with multiple structural anomalies, without...
5C50.02 — Embryofetopathy due to maternal phenylketonuria

ICD-11 5C50.02 — Embryofetopathy due to maternal phenylketonuria

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 such as heart defects (usually conotruncal), corpus callosus agenesis, neuronal migration disorders, facial dysmorphism and more rarely cleft palate, tracheo-oesophageal abnormalities.

The diagnosis includes nothing.

The diagnosis excludes nothing.

It has no clarifying diagnoses.

The diagnosis is coded elsewhere:

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