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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.