chromosome 11, deletion 11p

Preferred Label : chromosome 11, deletion 11p;

MeSH synonym : monosomy 11p; deletion 11p;

Is substance : O;

Origin ID

C538293;

UMLS CUI

C2931795;

CISMeF manual mappings
- Aniridia [ORDO Disease]
Currated CISMeF NLP mapping
- Absence of iris [ICD-10 Sub-category]
- Absence of iris [ICD-10 Sub-category (who)]
- Aniridia [PASCAL descriptor]
- Aniridia [NCIt concept]
- Aniridia [HPO term]
- Congenital aniridia (disorder) [SNOMED CT concept]
- aniridia [SNOMED Notion]
False automatic mappings
- Aniridia 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 11 [MeSH Descriptor]
ORDO relation(s)
- Aniridia [ORDO Disease]
Record concept(s)
- Chromosome 11, deletion 11p [MeSH concept]
See also (suggested by CISMeF)
- chromosome 11p deletion syndrome [MeSH Supplementary Concept]
See also inter- (CISMeF)
- aniridia [Disease (Nov.)]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Loss of Chromosome 11p [NCIt concept]