Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency

disorder

SNOMED 1351576009CUI C5968785

Overview

Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency is a disorder.

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

Related Conditions

Autosomal recessive hyper-IgM syndrome(parent)

CMMR-D (constitutional mismatch repair deficiency) syndrome(parent)

Quick Facts

SNOMED CT: 1351576009
UMLS CUI: C5968785
Fully Specified Name: Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency (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.