uniparental disomy, paternal, chromosome 14

Preferred Label : uniparental disomy, paternal, chromosome 14;

MeSH synonym : paternal uniparental disomy 14;

Origin ID

C536471;

UMLS CUI

C1842466;

CISMeF manual mappings
- Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14 [ORDO Disease]
Currated CISMeF NLP mapping
- Kagami-ogata syndrome [OMIM Phenotype]
- Paternal uniparental disomy of chromosome 14 [ICD-11 More detail]
- Uniparental disomy of paternal origin of chromosome 14 (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- Imprinting Disorders [MeSH Descriptor]
- chromosomes, human, pair 14 [MeSH Descriptor]
- uniparental disomy [MeSH Descriptor]
ORDO relation(s)
- Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14 [ORDO Disease]
Record concept(s)
- Kagami-Ogata syndrome [MeSH concept]
- Uniparental disomy, paternal, chromosome 14 [MeSH concept]
See also inter- (CISMeF)
- Kagami Ogata syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Kagami Ogata syndrome (disorder) [SNOMED CT concept]
- Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14 [ORDO Disease]
- Kagami-ogata syndrome [OMIM Phenotype]
- Uniparental disomy of paternal origin of chromosome 14 (disorder) [SNOMED CT concept]