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Arthrogryposis and ectodermal dysplasia syndrome
disorderSNOMED 786039009CUI C5191837
Overview
Arthrogryposis and ectodermal dysplasia syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Ectodermal dysplasia with hair-tooth-nail defects(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of the integument(parent)
Camptodactyly(parent)
Inherited arthrogryposis(parent)
Genetic disorder of nail(parent)
Hereditary disorder of tooth(parent)
Congenital deformity of hand(parent)
Distal arthrogryposis syndrome(parent)
Quick Facts
- SNOMED CT
- 786039009
- UMLS CUI
- C5191837
- Fully Specified Name
- Arthrogryposis and ectodermal dysplasia 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.