chromosome 3, monosomy 3p

Preferred Label : chromosome 3, monosomy 3p;

MeSH synonym : monosomy 3p; chromosome 3, deletion 3p; deletion 3p;

Origin ID

C536804;

UMLS CUI

C0795806;

Automatic exact mappings (from CISMeF team)
- Loss of Chromosome 3p [NCIt concept]
CISMeF manual mappings
- 3p partial monosomy syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Chromosome 3pter-p25 deletion syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 3 [MeSH Descriptor]
Record concept(s)
- Chromosome 3, monosomy 3p [MeSH concept]
See also inter- (CISMeF)
- Distal monosomy 3p [ORDO Disease]
- Distal monosomy 3p syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- 3p deletion syndrome [DO Concept]
- 3p partial monosomy syndrome (disorder) [SNOMED CT concept]
- Chromosome 3pter-p25 deletion syndrome [OMIM Phenotype]