Overview
Arthrogryposis multiplex congenita is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Adducted thumbs and arthrogryposis syndrome Christian type(child)
Arthrogryposis multiplex congenita and whistling face syndrome(child)
Arthrogryposis hyperkeratosis syndrome lethal form(child)
Vuopala disease(child)
Pena-Shokeir syndrome type I(child)
Autosomal recessive myogenic arthrogryposis multiplex congenita(child)
Congenital lethal myopathy Compton North type(child)
Neurogenic arthrogryposis multiplex congenita(child)
Hypomyelination neuropathy arthrogryposis syndrome(child)
X-linked distal arthrogryposis multiplex congenita(child)
Intellectual disability, developmental delay, contracture syndrome(child)
Marden Walker syndrome(child)
Kuskokwim syndrome(child)
Malignant hyperthermia with arthrogryposis and torticollis syndrome(child)
Van den Ende-Gupta syndrome(child)
Prenatal-onset spinal muscular atrophy with congenital bone fractures(child)
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome(child)
Microphthalmia, microtia, foetal akinesia syndrome(child)
Antenatal multi-minicore disease with arthrogryposis multiplex congenita(child)
Congenital muscular dystrophy with arthrogryposis multiplex congenita(child)
Quick Facts
- SNOMED CT
- 205402004
- UMLS CUI
- C5779613
- Fully Specified Name
- Arthrogryposis multiplex congenita (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.