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Amyotonia congenita

disorder
SNOMED 63135006CUI C0002735

Overview

Amyotonia congenita 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.

Neurogenic muscle atrophy, especially in the lower limbs
HP:0003202

Related Conditions

Disorder of neuromuscular transmission(parent)
Myoneural disorder(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of nervous system(parent)
Congenital disease(parent)
Hereditary disorder of musculoskeletal system(parent)

Quick Facts

SNOMED CT
63135006
UMLS CUI
C0002735
Fully Specified Name
Amyotonia congenita (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
1
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.