chromosome 15q13.3 microdeletion syndrome

Preferred Label : chromosome 15q13.3 microdeletion syndrome;

MeSH synonym : microdeletion 15q13.3 syndrome; 15q13.3 microdeletion syndrome; 15q13.3 microdeletion; chromosome 15q13.3 deletion syndrome;

Details

Origin ID

C567439;

UMLS CUI

C2677613;

Currated CISMeF NLP mapping
- 15q13.3 deletion [ICD-11 More detail]
- 15q13.3 microdeletion syndrome [ORDO Disease]
- Chromosome 15q13.3 deletion syndrome [OMIM Phenotype]
- Microdeletion of chromosome 15q13.3 (disorder) [SNOMED CT concept]
- chromosome 15q13.3 deletion syndrome [Disease (Nov.)]
- chromosome 15q13.3 microdeletion syndrome [DO Concept]
DO Cross reference
- chromosome 15q13.3 microdeletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- chromosomes, human, pair 15 [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- seizures [MeSH Descriptor]
Record concept(s)
- chromosome 15q13.3 microdeletion syndrome [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- 15q13.3 deletion [ICD-11 More detail]
- 15q13.3 microdeletion syndrome [ORDO Disease]
- Chromosome 15q13.3 deletion syndrome [OMIM Phenotype]
- Microdeletion of chromosome 15q13.3 (disorder) [SNOMED CT concept]
- chromosome 15q13.3 deletion syndrome [Disease (Nov.)]
- chromosome 15q13.3 microdeletion syndrome [DO Concept]

Keyword's position in hierarchy(ies) :

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