chromosome 3, monosomy 3q13

Preferred Label : chromosome 3, monosomy 3q13;

MeSH synonym : deletion 3q13; monosomy 3q13;

Is substance : O;

Origin ID

C536808;

UMLS CUI

C2931338;

CISMeF manual mappings
- 3q13 microdeletion syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- 3q13 deletion [ICD-11 More detail]
- 3q13 microdeletion syndrome (disorder) [SNOMED CT concept]
- Chromosome 3q13.31 deletion syndrome [OMIM Phenotype]
- chromosome 3q13.31 deletion syndrome [DO Concept]
DO Cross reference
- chromosome 3q13.31 deletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 3 [MeSH Descriptor]
ORDO relation(s)
- 3q13 microdeletion syndrome [ORDO Disease]
Record concept(s)
- Chromosome 3, monosomy 3q13 [MeSH 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]