Ehlers-Danlos syndrome, type 3

disorder

SNOMED 30652003CUI C0268337

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Arthralgias

Very frequent (80-99%)HP:0002829

Dislocated femoral heads

Very frequent (80-99%)HP:0002827

Extra bones within cranial sutures

Very frequent (80-99%)HP:0002645

Foot deformity

Very frequent (80-99%)HP:0001760

Joint dislocation

Very frequent (80-99%)HP:0001373

Ligamentous laxity

Very frequent (80-99%)HP:0001382

Muscle pain

Very frequent (80-99%)HP:0003326

Persistent blue colour of hands or feet

Very frequent (80-99%)HP:0001063

Skin hyperelasticity

Very frequent (80-99%)HP:0000974

Tiredness

Very frequent (80-99%)HP:0012378

Trouble sleeping

Very frequent (80-99%)HP:0002360

Ulnohumeral dislocation

Very frequent (80-99%)HP:0003042

Vertigo

Very frequent (80-99%)HP:0002321

Arachnodactyly

Frequent (30-79%)HP:0001166

Bruising susceptibility

Frequent (30-79%)HP:0000978

Cardiac arrhythmias

Frequent (30-79%)HP:0011675

Chronic pain

Frequent (30-79%)HP:0012532

Decreased nerve conduction velocity

Frequent (30-79%)HP:0000762

Dental crowding

Frequent (30-79%)HP:0000678

Depression

Frequent (30-79%)HP:0000716

Dyschezia

Frequent (30-79%)HP:0002019

Excessive, persistent worry and fear

Frequent (30-79%)HP:0000739

Fallen arches

Frequent (30-79%)HP:0001763

Intermittent migraine headaches

Frequent (30-79%)HP:0002076

Intestinal malabsorption

Frequent (30-79%)HP:0002024

Mitral valve prolapse

Frequent (30-79%)HP:0001634

Muscle pain with exercise

Frequent (30-79%)HP:0003738

Nausea and vomiting

Frequent (30-79%)HP:0002017

Osteoarthritis

Frequent (30-79%)HP:0002758

Pelvic organ prolapse

Frequent (30-79%)HP:0031607

Related Conditions

Hypermobility syndrome(parent)

Ehlers-Danlos syndrome(parent)

Congenital anomaly of bone and joint(parent)

Lesion of joint(parent)

Autosomal hereditary disorder(parent)

Quick Facts

SNOMED CT: 30652003
UMLS CUI: C0268337
Fully Specified Name: Hypermobile Ehlers-Danlos syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.