← Back to Conditions

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.

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.

Classical phenylketonuria with total deficiency of phenylalanine hydroxylase — Symptoms, Testing & Specialists | Ltrl | Ltrl