chromosome 1q21.1 deletion syndrome, 1.35-Mb

Preferred Label : chromosome 1q21.1 deletion syndrome, 1.35-Mb;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0567591;

UMLS CUI

C2675897;

Currated CISMeF NLP mapping
- 1q21.1 deletion [ICD-11 More detail]
- 1q21.1 deletion syndrome [Disease (Nov.)]
- 1q21.1 microdeletion syndrome [ORDO Disease]
- 1q21.1 microdeletion syndrome (disorder) [SNOMED CT concept]
- Chromosome 1q21.1 deletion syndrome, 1.35-mb [OMIM Phenotype]
- chromosome 1q21.1 deletion syndrome [DO Concept]
Related record
- chromosome 1q21.1 deletion syndrome, 1.35-Mb [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- 1q21.1 deletion [ICD-11 More detail]
- 1q21.1 deletion syndrome [Disease (Nov.)]
- 1q21.1 microdeletion syndrome [ORDO Disease]
- 1q21.1 microdeletion syndrome (disorder) [SNOMED CT concept]
- Chromosome 1q21.1 deletion syndrome, 1.35-mb [OMIM Phenotype]
- chromosome 1q21.1 deletion syndrome [DO Concept]