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Familial congenital controlateral synkinesia

disorder
SNOMED 784348007CUI C5191311

Overview

Familial congenital controlateral synkinesia 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.

Abnormality of movement
Frequent (30-79%)HP:0100022
Clumsiness
Frequent (30-79%)HP:0002312
Easy fatigability
Frequent (30-79%)HP:0003388
Fine motor skill dysfunction
Frequent (30-79%)HP:0007010
Involvement of the corticospinal pathways
Frequent (30-79%)HP:0002492
Mirror movements
Frequent (30-79%)HP:0001335
Absence of corpus callosum
Occasional (5-29%)HP:0001274
Hippocampal dysgenesis
Occasional (5-29%)HP:0025101
Muscle pain
Occasional (5-29%)HP:0003326
Specific learning disability
Occasional (5-29%)HP:0001328
CP
Very rare (1-4%)HP:0100021
Fused neck
Very rare (1-4%)HP:0002949
Low gonadotropins (secondary hypogonadism)
Very rare (1-4%)HP:0000044
Mental retardation, mild
Very rare (1-4%)HP:0001256

Related Conditions

Hereditary disorder of nervous system(parent)
Congenital disease(parent)
Autosomal hereditary disorder(parent)
Familial disease(parent)
Mirror movements(parent)

Quick Facts

SNOMED CT
784348007
UMLS CUI
C5191311
Fully Specified Name
Familial congenital mirror movements (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
14
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.