Overview
X-linked dominant hereditary disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
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X-linked intellectual disability Atkin type(child)
Aicardi's syndrome(child)
Alport syndrome X-linked(child)
CASK - Calcium/calmodulin-dependent serine protein kinase related intellectual disability(child)
Craniofrontonasal dysplasia(child)
Fragile X syndrome(child)
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Fragile X associated tremor ataxia syndrome(child)
Quick Facts
- SNOMED CT
- 1162984000
- UMLS CUI
- C5566661
- Fully Specified Name
- X-linked dominant hereditary disease (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.