Uniparental disomy, paternal, chromosome 14

Preferred Label : Uniparental disomy, paternal, chromosome 14;

UMLS semantic type : T049 - Cell or Molecular Dysfunction;

Origin ID

M0530932;

UMLS CUI

C1842466;

Currated CISMeF NLP mapping
- Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14 [ORDO Disease]
- 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 narrower concept(s)
- Kagami-Ogata syndrome [MeSH concept]
Related record
- uniparental disomy, paternal, chromosome 14 [MeSH Supplementary 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]