Potassium voltage-gated channel subfamily Q member 2 developmental and epileptic encephalopathy

disorder

SNOMED 778001003CUI C4755256

Overview

Potassium voltage-gated channel subfamily Q member 2 developmental and epileptic encephalopathy is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Neonatal disease(parent)

Developmental hereditary disorder(parent)

DEE - developmental and epileptic encephalopathy(parent)

Quick Facts

SNOMED CT: 778001003
UMLS CUI: C4755256
Fully Specified Name: Potassium voltage-gated channel subfamily Q member 2 developmental and epileptic encephalopathy (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.