chromosome 11p deletion syndrome

Preferred Label : chromosome 11p deletion syndrome;

MeSH synonym : 11p deletion syndrome;

Origin ID

C541598;

UMLS CUI

C0812435;

Automatic exact mappings (from CISMeF team)
- Chromosome 11p11.2 deletion syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 11 [MeSH Descriptor]
- wagr syndrome [MeSH Descriptor]
Record concept(s)
- Chromosome 11p Deletion Syndrome [MeSH concept]
See also (suggested by CISMeF)
- chromosome 11, deletion 11p [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]