AMRF - action myoclonus renal failure

disorder

SNOMED 764453009CUI C0751779

Overview

AMRF - action myoclonus renal failure 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.

Edema

Always present (100%)HP:0000969

Hypoalbuminaemia

Always present (100%)HP:0003073

Jerking

Always present (100%)HP:0001336

Nephrosis

Always present (100%)HP:0000100

Normochromic anaemia

Always present (100%)HP:0001895

Proteinuria

Always present (100%)HP:0000093

Renal failure

Always present (100%)HP:0000083

Anasarca

Frequent (30-79%)HP:0012050

Deglutition disorder

Frequent (30-79%)HP:0002015

Fluid around lungs

Frequent (30-79%)HP:0002202

Thrombocytopenia

Frequent (30-79%)HP:0001873

Unsteady walk

Frequent (30-79%)HP:0002317

Action tremor

HP:0002345

Atrophic cerebellum

HP:0001272

Cerebellar tremor

HP:0002080

Difficulty articulating speech

HP:0001260

Focal and segmental glomerulosclerosis

HP:0000097

Generalised-onset seizure

HP:0002197

Glomerulopathy

HP:0100820

Inability to coordinate movements when walking

HP:0002066

Intellectual deterioration

Excluded (<1%)HP:0001268

Kidney damage

HP:0000112

Postural tremor

HP:0002174

Related Conditions

Congenital disease(parent)

Recessive hereditary disorder (autosomal)(parent)

Progressive myoclonic epilepsy(parent)

Hereditary disorder of nervous system(parent)

Quick Facts

SNOMED CT: 764453009
UMLS CUI: C0751779
Fully Specified Name: Action myoclonus renal failure syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 23

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.