Ehlers-Danlos syndrome classic type

disorder

SNOMED 715318006CUI C4225429

Overview

Ehlers-Danlos syndrome classic type 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.

Cigarette-paper scars

Very frequent (80-99%)HP:0001073

Fragile skin

Very frequent (80-99%)HP:0001030

Generalized joint laxity

Very frequent (80-99%)HP:0002761

Skin hyperelasticity

Very frequent (80-99%)HP:0000974

Soft, doughy skin

Very frequent (80-99%)HP:0001027

Striae atrophicae

Very frequent (80-99%)HP:0001065

Thin, atrophic scars

Very frequent (80-99%)HP:0001075

Chronic constipation

Frequent (30-79%)HP:0012450

Gastro-esophageal reflux

Frequent (30-79%)HP:0002020

Muscle spasm

Frequent (30-79%)HP:0003394

Muscle weakness

Frequent (30-79%)HP:0001324

Nausea

Frequent (30-79%)HP:0002018

Osteopenia

Frequent (30-79%)HP:0000938

Peripheral hypotonia

Frequent (30-79%)HP:0001252

Poor wound healing

Frequent (30-79%)HP:0001058

Pulpoliths

Frequent (30-79%)HP:0003771

Tiredness

Frequent (30-79%)HP:0012378

Vomiting

Frequent (30-79%)HP:0002013

Abnormal heart valve physiology

Occasional (5-29%)HP:0031653

Abnormality of the feet

Occasional (5-29%)HP:0001760

Arterial dissection

Occasional (5-29%)HP:0005294

Arterial rupture

Occasional (5-29%)HP:0025019

Arteriovenous fistula

Occasional (5-29%)HP:0004947

Arthritic pain

Occasional (5-29%)HP:0002829

Bladder diverticulum

Occasional (5-29%)HP:0000015

Bruising susceptibility

Occasional (5-29%)HP:0000978

Cerebral aneurysm

Occasional (5-29%)HP:0004944

Cervical insufficiency

Occasional (5-29%)HP:0030009

Cornela disease

Occasional (5-29%)HP:0000481

Dermatochalasis

Occasional (5-29%)HP:0010750

Related Conditions

Ehlers-Danlos syndrome classic type 2(child)

Autosomal dominant hereditary disorder(parent)

Ehlers-Danlos syndrome(parent)

Quick Facts

SNOMED CT: 715318006
UMLS CUI: C4225429
Fully Specified Name: Ehlers-Danlos syndrome classic type (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.