Chromosome 3, monosomy 3q13

Preferred Label : Chromosome 3, monosomy 3q13;

UMLS semantic type : T049 - Cell or Molecular Dysfunction;

Origin ID

M0531269;

UMLS CUI

C2931338;

Currated CISMeF NLP mapping
- 3q13 deletion [ICD-11 More detail]
- 3q13 microdeletion syndrome [ORDO Disease]
- 3q13 microdeletion syndrome (disorder) [SNOMED CT concept]
- Chromosome 3q13.31 deletion syndrome [OMIM Phenotype]
- chromosome 3q13.31 deletion syndrome [DO Concept]
Related record
- chromosome 3, monosomy 3q13 [MeSH Supplementary Concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- 3q13 microdeletion syndrome [ORDO Disease]
- 3q13 microdeletion syndrome (disorder) [SNOMED CT concept]
- chromosome 3q13.31 deletion syndrome [DO Concept]