Epidermal growth factor-related primary hypomagnesaemia with intellectual disability

disorder

SNOMED 1351962002CUI C5681825

Overview

Epidermal growth factor-related primary hypomagnesaemia with intellectual disability is a disorder.

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

Related Conditions

Metabolic renal disease(parent)

Developmental hereditary disorder(parent)

Hereditary nephropathy(parent)

Primary hypomagnesemia(parent)

Recessive hereditary disorder (autosomal)(parent)

Renal tubular disorder(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 1351962002
UMLS CUI: C5681825
Fully Specified Name: Epidermal growth factor-related primary hypomagnesemia with intellectual disability (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.