chromosome 8, monosomy 8p23 1

Preferred Label : chromosome 8, monosomy 8p23 1;

MeSH synonym : monosomy 8p23 1; deletion 8p23 1;

Is substance : O;

Origin ID

C537827;

UMLS CUI

C2931638;

Currated CISMeF NLP mapping
- 8p23.1 deletion [ICD-11 More detail]
- 8p23.1 microdeletion syndrome [ORDO Disease]
- 8p23.1 microdeletion syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 8 [MeSH Descriptor]
Record concept(s)
- Chromosome 8, monosomy 8p23 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 8p23.1 deletion [ICD-11 More detail]
- 8p23.1 microdeletion syndrome [ORDO Disease]
- 8p23.1 microdeletion syndrome (disorder) [SNOMED CT concept]