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X-linked retinitis pigmentosa

disorder
SNOMED 232054005CUI C0339528

Overview

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

Related Conditions

Chromosome Xp11.3 microdeletion syndrome(child)
X-linked retinitis pigmentosa heterozygote(child)
Primary ciliary dyskinesia and retinitis pigmentosa syndrome(child)
Retinitis pigmentosa(parent)
X-linked hereditary disease(parent)

Quick Facts

SNOMED CT
232054005
UMLS CUI
C0339528
Fully Specified Name
X-linked retinitis pigmentosa (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.