Overview
Dysostosis multiplex group is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
GM1 gangliosidosis(child)
Sialic storage disease(child)
Combined deficiency of sialidase AND beta galactosidase(child)
Mannosidosis(child)
I-cell disease(child)
Dysostosis multiplex(child)
Mucopolysaccharidosis-like syndrome with congenital heart defect and hematopoietic disorder(child)
Disorder of lysosomal enzyme(parent)
Skeletal dysplasia(parent)
Metabolic bone disease(parent)
Congenital anomaly of skeletal bone(parent)
Quick Facts
- SNOMED CT
- 279081001
- UMLS CUI
- C0458249
- Fully Specified Name
- Dysostosis multiplex group (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.