← Back to Conditions
Hereditary disorder of musculoskeletal system
disorderSNOMED 363212003CUI C1285363
Overview
Hereditary disorder of musculoskeletal system is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Craniodiaphyseal dysplasia(child)
Mandibuloacral dysostosis(child)
Myoclonic epilepsy with ragged red fibers(child)
Lipid storage myopathy(child)
Geroderma osteodysplastica(child)
Triglyceride storage disease with ichthyosis(child)
Pyle metaphyseal dysplasia(child)
Morquio syndrome(child)
Papillon-Lefèvre syndrome(child)
Muscle L-lactate dehydrogenase deficiency(child)
Rhizomelic chondrodysplasia punctata syndrome(child)
Congenital myotonia, autosomal dominant form(child)
Menkes kinky-hair syndrome(child)
Muscle phosphoglycerate mutase deficiency(child)
Robinow syndrome(child)
Muscle AMP deaminase deficiency(child)
Autosomal dominant hypophosphataemic bone disease(child)
Autosomal recessive hypophosphatemic bone disease(child)
Nail-patella syndrome(child)
Inherited arthrogryposis(child)
Quick Facts
- SNOMED CT
- 363212003
- UMLS CUI
- C1285363
- Fully Specified Name
- Hereditary disorder of musculoskeletal system (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.