Tetrasomy 18p - CISMeF

Preferred Label : Tetrasomy 18p;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Isochromosome 18p syndrome;

Prefixed ID : #614290;

Details

Origin ID

614290;

UMLS CUI

C0795868;

Currated CISMeF NLP mapping
- Chromosome 18, tetrasomy 18p [MeSH concept]
- Tetrasomy 18p [ICD-11 More detail]
- Tetrasomy 18p [ORDO Disease]
- Tetrasomy 18p (disorder) [SNOMED CT concept]
- chromosome 18, tetrasomy 18p [MeSH Supplementary Concept]
ORDO concept(s)
- Tetrasomy 18p [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome 18, tetrasomy 18p [MeSH concept]
- Tetrasomy 18p [ORDO Disease]
- Tetrasomy 18p (disorder) [SNOMED CT concept]
- chromosome 18, tetrasomy 18p [MeSH Supplementary Concept]

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