Xp11.3 deletion - CISMeF

" /> Xp11.3 deletion - CISMeF

CISMeF

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Xp11.3 deletionICD-11 More detail

Preferred Label : Xp11.3 deletion;

Details

Origin ID

1764087058;

UMLS CUI

C1845136;

CISMeF manual mappings
- chromosome Xp11.3 deletion syndrome [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Chromosome xp11.3 deletion syndrome [OMIM Phenotype]
- Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3 [ORDO Disease]
- chromosome Xp11.3 deletion syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome xp11.3 deletion syndrome [OMIM Phenotype]
- Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3 [ORDO Disease]
- chromosome Xp11.3 deletion syndrome [MeSH concept]
- chromosome Xp11.3 deletion syndrome [MeSH Supplementary Concept]

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06/05/2025

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