chromosome 9, partial monosomy 9p

Preferred Label : chromosome 9, partial monosomy 9p;

MeSH synonym : 9p- syndrome, partial; distal monosomy 9p; partial deletion of short arm of chromosome 9; 9p partial monosomy; deletion 9p syndrome, partial;

Détails

Origin ID

C538025;

UMLS CUI

C0265425;

Automatic exact mappings (from CISMeF team)
- Chromosome 9p deletion syndrome [OMIM Phenotype]
CISMeF manual mappings
- 9p partial monosomy syndrome [SNOMED Notion]
- Distal monosomy 9p [ORDO Disease]
Currated CISMeF NLP mapping
- 9p partial monosomy syndrome (disorder) [Inactive SNOMED CT concept]
- Distal monosomy 9p syndrome (disorder) [SNOMED CT concept]
- Partial deletion of the short arm of chromosome 9 [ORDO Disease]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 9 [MeSH Descriptor]
Record concept(s)
- Chromosome 9, partial monosomy 9p [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 9p partial monosomy syndrome [SNOMED Notion]
- 9p partial monosomy syndrome (disorder) [Inactive SNOMED CT concept]
- Distal monosomy 9p [ORDO Disease]
- Distal monosomy 9p syndrome (disorder) [SNOMED CT concept]
- Partial deletion of the short arm of chromosome 9 [ORDO Disease]

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