Rambaud Gallian syndrome

disorder

SNOMED 724002003CUI C4510224

Overview

Rambaud Gallian syndrome is a disorder.

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

Related Conditions

Cerebral calcification(parent)

Retinal ischemia(parent)

Recessive hereditary disorder (autosomal)(parent)

Vascular degeneration(parent)

Cardiovascular system hereditary disorder(parent)

Hereditary disorder of the visual system(parent)

Hereditary degenerative disease of central nervous system(parent)

Quick Facts

SNOMED CT: 724002003
UMLS CUI: C4510224
Fully Specified Name: Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (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.