Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase

disorder

SNOMED 890435004CUI C5438321

Overview

Classical phenylketonuria with partial 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: 890435004
UMLS CUI: C5438321
Fully Specified Name: Classical phenylketonuria with partial 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 partial deficiency of phenylalanine hydroxylase — Symptoms, Testing & Specialists | Ltrl