Overview
Anomaly of chromosome X is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Fragile X chromosome(child)
Trisomy X syndrome(child)
Turner syndrome(child)
XXXXY syndrome(child)
XX males(child)
XXXY syndrome(child)
Four X syndrome(child)
Penta X syndrome(child)
Klinefelter syndrome(child)
Chromosome Xq27.3q28 duplication syndrome(child)
Chromosome Xp11.3 microdeletion syndrome(child)
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome(child)
Microduplication Xp11.22p11.23 syndrome(child)
X-linked diffuse leiomyomatosis with Alport syndrome(child)
Chromosome Xp22.3 microdeletion syndrome(child)
Atypical Norrie disease due to monosomy Xp11.3(child)
Xq12-q13.3 duplication syndrome(child)
X small rings(child)
Intellectual disability, seizures, macrocephaly, obesity syndrome(child)
49,XXXYY syndrome(child)
Quick Facts
- SNOMED CT
- 111312006
- UMLS CUI
- C0265495
- Fully Specified Name
- Anomaly of chromosome X (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.