Adenine phosphoribosyl transferase deficiency type II

disorder

SNOMED 238010006CUI C0342799

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Deficiency of AMP pyrophorylase(parent)

Quick Facts

SNOMED CT: 238010006
UMLS CUI: C0342799
Fully Specified Name: Adenine phosphoribosyl transferase deficiency type II (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.