Related Conditions
Triploidy, diploidy, mixoploidy syndrome(child)
Duplication seen only at prometaphase(child)
Duplication with other complex rearrangement(child)
Triploidy and polyploidy(child)
Trisomy and partial trisomy of autosome(child)
Anomaly of chromosome pair(child)
Pseudotrisomy 18(child)
XXYY syndrome(child)
Chimera(child)
Group chromosomal alteration(child)
Polyploidy syndrome(child)
Mosaic variegated aneuploidy syndrome(child)
Der(22) syndrome due to 3:1 meiotic disjunction events(child)
Ring chromosome(child)
Congenital disease(parent)
Chromosomal disorder(parent)
Quick Facts
- SNOMED CT
- 74345006
- UMLS CUI
- C0008626
- Fully Specified Name
- Congenital disorder due to abnormality of chromosome number OR structure (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.