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Ehlers-Danlos and osteogenesis imperfecta syndrome
disorderSNOMED 733457006CUI C4518787
Overview
Ehlers-Danlos and osteogenesis imperfecta syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Autosomal dominant hereditary disorder(parent)
Osteogenesis imperfecta(parent)
Connective tissue hereditary disorder(parent)
Hereditary disorder of the integument(parent)
Hereditary disorder of musculoskeletal system(parent)
Congenital anomaly of skin(parent)
Dysplasia with decreased bone density(parent)
Musculoskeletal and connective tissue disorder(parent)
Congenital connective tissue disorder(parent)
Developmental hereditary disorder(parent)
Movement disorder(parent)
Skin lesion(parent)
Arthropathy(parent)
Quick Facts
- SNOMED CT
- 733457006
- UMLS CUI
- C4518787
- Fully Specified Name
- Ehlers-Danlos and osteogenesis imperfecta syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.