Atypical Norrie disease due to monosomy Xp11.3

disorder

SNOMED 733626002CUI C4518083

Overview

Atypical Norrie disease due to monosomy Xp11.3 is a disorder.

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

Related Conditions

Anomaly of chromosome X(parent)

Congenital anomaly of retina(parent)

Multiple system malformation syndrome(parent)

Quick Facts

SNOMED CT: 733626002
UMLS CUI: C4518083
Fully Specified Name: Atypical Norrie disease due to monosomy Xp11.3 (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.