Overview
Chondrodysplasia punctata is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Chondrodysplasia punctata, X-linked recessive type(child)
Chondrodysplasia punctata, MT type(child)
Rhizomelic chondrodysplasia punctata syndrome(child)
Hyperphosphatasia-osteoectasia syndrome(child)
Chondrodysplasia punctata, Conradi-Hünermann type(child)
Chondrodysplasia punctata, X-linked dominant type(child)
Chondrodysplasia punctata Toriello type(child)
Lissencephaly type 3 metacarpal bone dysplasia syndrome(child)
Brachytelephalangic chondrodysplasia punctata(child)
Chondrodysplasia punctata due to maternal autoimmune disease(child)
Skeletal dysplasia(parent)
Congenital anomaly of skeletal bone(parent)
Quick Facts
- SNOMED CT
- 278715001
- UMLS CUI
- C0008445
- Fully Specified Name
- Chondrodysplasia punctata (stippled epiphyses) 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.