Overview
Distal arthrogryposis syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Distal arthrogryposis type 2B(child)
Distal arthrogryposis type 5(child)
Distal arthrogryposis type 4(child)
Digitotalar dysmorphism(child)
Distal arthrogryposis type 6(child)
Ehlers-Danlos syndrome musculocontractural type(child)
Freeman-Sheldon syndrome(child)
Autism spectrum disorder, epilepsy, arthrogryposis syndrome(child)
Distal arthrogryposis type 8(child)
Distal arthrogryposis type 5D(child)
Pelvic dysplasia, arthrogryposis of lower limbs syndrome(child)
Distal arthrogryposis type 3(child)
Congenital plantar flexion contracture(child)
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome(child)
CCA - Congenital contractural arachnodactyly(child)
Arthrogryposis and ectodermal dysplasia syndrome(child)
Hecht syndrome(child)
Arthrogryposis(parent)
Genetic disease(parent)
Quick Facts
- SNOMED CT
- 24269006
- UMLS CUI
- C0265213
- Fully Specified Name
- Distal arthrogryposis 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.