Classical phenylketonuria with total deficiency of phenylalanine hydroxylase

disorder

SNOMED 890436003CUI C5438322

Overview

Classical phenylketonuria with total deficiency of phenylalanine hydroxylase is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Classical phenylketonuria(parent)

Quick Facts

SNOMED CT: 890436003
UMLS CUI: C5438322
Fully Specified Name: Classical phenylketonuria with total deficiency of phenylalanine hydroxylase (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.