Maternal uniparental disomy of chromosome 13 - CISMeF

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CISMeF

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Maternal uniparental disomy of chromosome 13ICD-11 More detail

Preferred Label : Maternal uniparental disomy of chromosome 13;

Details

Origin ID

729188840;

Currated CISMeF NLP mapping
- Maternal uniparental disomy of chromosome 13 [ORDO Disease]
- Maternal uniparental disomy of chromosome 13 (disorder) [SNOMED CT concept]
Validated automatic mappings to NTBT
- uniparental disomy of 13 [MeSH Supplementary Concept]

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03/05/2025

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