Classical-like Ehlers-Danlos syndrome type 2

disorder

SNOMED 1255121003CUI C4693870

Overview

Classical-like Ehlers-Danlos syndrome type 2 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.

Atypical scarring

Always present (100%)HP:0000987

Chronic extreme exhaustion

Always present (100%)HP:0012432

Decreased dermal collagen

Always present (100%)HP:0034943

Generalized joint laxity

Always present (100%)HP:0002761

Intermittent claudication

Always present (100%)HP:0004417

Klippel-Feil syndrome

Always present (100%)HP:0004602

Low back pain

Always present (100%)HP:0003419

Molluscoid pseudotumor

Always present (100%)HP:0000993

Osteoarthritis

Always present (100%)HP:0002758

Poor wound healing

Always present (100%)HP:0001058

Premature sagging cheeks

Always present (100%)HP:0034273

Prematurely aged appearance

Always present (100%)HP:0007495

Prominent veins

Always present (100%)HP:0001015

Recurrent patellar dislocation

Always present (100%)HP:0005001

Recurrent thrombosis

Always present (100%)HP:0004419

Soft, doughy skin

Always present (100%)HP:0001027

Thin, atrophic scars

Always present (100%)HP:0001075

Abnormality of the feet

Very frequent (80-99%)HP:0001760

Bruising susceptibility

Very frequent (80-99%)HP:0000978

Bunion

Very frequent (80-99%)HP:0001822

Fallen arches

Very frequent (80-99%)HP:0001763

Hammertoe

Very frequent (80-99%)HP:0001765

Joint dislocation

Very frequent (80-99%)HP:0001373

Loose redundant skin

Very frequent (80-99%)HP:0001582

Loose-jointedness

Very frequent (80-99%)HP:0001382

Osteopenia

Very frequent (80-99%)HP:0000938

Skin hyperelasticity

Very frequent (80-99%)HP:0000974

Widened atrophic scar

Very frequent (80-99%)HP:0031158

Dislocated femoral heads

Frequent (30-79%)HP:0002827

Dislocations of the knees

Frequent (30-79%)HP:0004976

Related Conditions

Dysplasia with decreased bone density(parent)

Ehlers-Danlos syndrome(parent)

Recurrent dislocation of joint(parent)

Movement disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1255121003
UMLS CUI: C4693870
Fully Specified Name: Classical-like Ehlers-Danlos syndrome type 2 (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.