MeSH Browser

MeSH Supplementary: Homozygous 11p15-p14 Deletion Syndrome
Unique ID: C564701
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564701
Entry Term(s): Hyperinsulinism, Infantile, with Enteropathy and Deafness
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 11; *Hearing Loss, Sensorineural; *Hyperinsulinism; *Intestinal Diseases
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Homozygous 11p15-p14 Deletion Syndrome MeSH Supplementary Concept Data 2024