Stark Kaeser syndrome

disorder

SNOMED 1208615009CUI C1867005

Overview

Stark Kaeser syndrome 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 scapuloperoneal syndrome

Very frequent (80-99%)HP:0003704

Shoulder girdle muscle wasting

Very frequent (80-99%)HP:0003724

Gynaecomastia

Frequent (30-79%)HP:0000771

Rimmed vacuoles

Frequent (30-79%)HP:0003805

Z-band streaming

Frequent (30-79%)HP:0020203

Deglutition disorder

Occasional (5-29%)HP:0002015

Inability to heel walk

Occasional (5-29%)HP:0009027

Weakness of face

Occasional (5-29%)HP:0030319

Foot, talipes equinovarus

HP:0001762

Peroneal muscle atrophy

HP:0009049

Related Conditions

Autosomal dominant hereditary disorder(parent)

Myoneural disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Familial motor neuron disease(parent)

Atrophy of muscle of shoulder(parent)

Atrophy of peroneal muscle(parent)

Quick Facts

SNOMED CT: 1208615009
UMLS CUI: C1867005
Fully Specified Name: Neurogenic scapuloperoneal syndrome Kaeser type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.