uniparental disomy of 13

Preferred Label : uniparental disomy of 13;

CISMeF synonym : maternal uniparental disomy of chromosome 13; paternal uniparental disomy of chromosome 13;

MeSH synonym : uniparental disomy of chromosome 13;

MeSH hyponym : Paternal uniparental disomy 13; Maternal uniparental disomy 13;

Is substance : O;

Details

Origin ID

C536469;

UMLS CUI

C2931198;

CISMeF manual mappings
- Maternal uniparental disomy of chromosome 13 [ORDO Disease]
- Paternal uniparental disomy of chromosome 13 [ORDO Disease]
Currated CISMeF NLP mapping
- Paternal uniparental disomy of chromosome 13 [ICD-11 More detail]
- Uniparental disomy of chromosome 13 [ORDO Disease]
MeSH term(s) associated for indexing
- chromosomes, human, pair 13 [MeSH Descriptor]
- uniparental disomy [MeSH Descriptor]
Record concept(s)
- Maternal uniparental disomy of chromosome 13 [MeSH concept]
- Paternal uniparental disomy of chromosome 13 [MeSH concept]
- Uniparental disomy of 13 [MeSH concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Maternal uniparental disomy of chromosome 13 [ORDO Disease]
- Paternal uniparental disomy of chromosome 13 [ORDO Disease]
- Uniparental disomy of chromosome 13 [ORDO Disease]
Validated automatic mappings to BTNT
- Maternal uniparental disomy of chromosome 13 [ICD-11 More detail]
- Maternal uniparental disomy of chromosome 13 (disorder) [SNOMED CT concept]
- Paternal uniparental disomy of chromosome 13 (disorder) [SNOMED CT concept]

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