Congenital elevation of scapula

disorder

SNOMED 79120002CUI C0152438

Overview

Congenital elevation of scapula 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 shoulder musculature

Very frequent (80-99%)HP:0001435

Abnormality of the shoulder

Very frequent (80-99%)HP:0003043

Short neck

Very frequent (80-99%)HP:0000470

Shoulder muscle hypoplasia

Very frequent (80-99%)HP:0008952

Spasmodic torticollis

Very frequent (80-99%)HP:0000473

Cleft of palate

Occasional (5-29%)HP:0000175

Cervical segmentation defect

HP:0004632

Hemivertebra

HP:0002937

Rib segmentation abnormalities

HP:0006655

Scoliosis

HP:0002650

Spina bifida occulta

HP:0003298

Sprengel deformity

HP:0000912

Underdevelopment of neck muscle

HP:0008984

Related Conditions

Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome(child)

Congenital elevation of right scapula(child)

Congenital elevation of left scapula(child)

Congenital anomaly of scapula(parent)

Displacement of bone(parent)

Quick Facts

SNOMED CT: 79120002
UMLS CUI: C0152438
Fully Specified Name: Congenital elevation of scapula (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.