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Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene
disorderSNOMED 1366635006CUI C6009956
Overview
Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Quick Facts
- SNOMED CT
- 1366635006
- UMLS CUI
- C6009956
- Fully Specified Name
- Polycystic liver disease-3 due to heterozygous mutation of ALG8 alpha-1,3-glucosyltransferase gene (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.