Diaphragmatic paresis

finding

SNOMED 95438009CUI C0521532

Overview

Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.

Associated Conditions

Conditions associated with this symptom based on HPO disease-phenotype annotations.

Charcot-Marie-Tooth disease, type IA

Occasional (5-29%)

Steinert myotonic dystrophy syndrome

Occasional (5-29%)

Fazio-Londe syndrome

Scapuloperoneal spinal muscular atrophy

Congenita hypotonic - sclerotic muscular dystrophy

Frequent (30-79%)

Glycogen heart disease

MPRM - myopathy, proximal, with early respiratory muscle involvement

Distal spinal muscular atrophy type 1

Autosomal dominant Charcot-Marie-Tooth disease type 2C

Congenital muscular dystrophy type 1B

Autosomal recessive distal spinal muscular atrophy type 3

EMARDD (early-onset myopathy, areflexia, respiratory distress, dysphagia) syndrome

Ventilator-induced diaphragmatic dysfunction

Very frequent (80-99%)

Related Symptoms

Abnormal diaphragmatic movement Spinal hemiparesis Spinal paraparesis Neurological muscle weakness Diaphragmatic breathing Singultus Normal diaphragmatic movement Paradoxical diaphragmatic movement Diaphragmatic tonic spasm Diaphragmatic tic

Quick Facts

SNOMED CT: 95438009
UMLS CUI: C0521532
Fully Specified Name: Diaphragmatic paresis (finding)
Associated Conditions: 16
Diagnostic Tests: 0

This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.