homozygous 11p15-p14 deletion syndrome

Preferred Label : homozygous 11p15-p14 deletion syndrome;

MeSH synonym : hyperinsulinism, infantile, with enteropathy and deafness;

Origin ID

C564701;

UMLS CUI

C1847866;

Currated CISMeF NLP mapping
- Homozygous 11p15-p14 deletion syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 11 [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
- hyperinsulinism [MeSH Descriptor]
- intestinal diseases [MeSH Descriptor]
Record concept(s)
- homozygous 11p15-p14 deletion syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Homozygous 11p15-p14 deletion syndrome [OMIM Phenotype]