chromosome 2q32-Q33 deletion syndrome

Preferred Label : chromosome 2q32-Q33 deletion syndrome;

Origin ID

C567350;

UMLS CUI

C2676739;

Currated CISMeF NLP mapping
- 2q32q33 deletion [ICD-11 More detail]
- 2q32q33 microdeletion syndrome [ORDO Disease]
- 2q32q33 microdeletion syndrome (disorder) [SNOMED CT concept]
- Glass syndrome [OMIM Phenotype]
- SATB2-associated syndrome [DO Concept]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 2 [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
Record concept(s)
- chromosome 2q32-Q33 deletion syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 2q32q33 microdeletion syndrome [ORDO Disease]
- Glass syndrome [OMIM Phenotype]
- SATB2-associated syndrome [DO Concept]