Familial cortical myoclonus

disorder

SNOMED 763770005CUI C3539916

Overview

Familial cortical myoclonus is a disorder.

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Action myoclonus

Always present (100%)HP:0034360

Fragmented sleep

Very frequent (80-99%)HP:0100785

Ataxia

Frequent (30-79%)HP:0001251

Frequent falls

Frequent (30-79%)HP:0002359

Ataxic tremor

Occasional (5-29%)HP:0002345

Jerking

HP:0001336

Related Conditions

Autosomal dominant hereditary disorder(parent)

Familial disease(parent)

Hereditary disorder of nervous system(parent)

Cerebral cortex myoclonus(parent)

Quick Facts

SNOMED CT: 763770005
UMLS CUI: C3539916
Fully Specified Name: Familial myoclonus of cerebral cortex (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.