Overview
Craniosynostosis fibular aplasia syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Multiple malformation syndrome with limb defect as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital anomaly of bone and joint(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)
Agenesis of fibula(parent)
Congenital synostosis of coronal suture of skull(parent)
Quick Facts
- SNOMED CT
- 732250002
- UMLS CUI
- C4517333
- Fully Specified Name
- Craniosynostosis fibular aplasia 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.