Atypical hypotonia cystinuria syndrome

disorder

SNOMED 778025006CUI C4755274

Overview

Atypical hypotonia cystinuria syndrome is a disorder.

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

Related Conditions

Cystinuria, type 1(parent)

Developmental hereditary disorder(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 778025006
UMLS CUI: C4755274
Fully Specified Name: Atypical hypotonia cystinuria 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.