MeSH Browser

MeSH Supplementary: Chromosome 17q21.31 Deletion Syndrome
Unique ID: C566476
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566476
Entry Term(s): 17q21.31 Deletion Syndrome; 17q21.31 Microdeletion Syndrome; Chromosome 17q21.31 Microdeletion Syndrome; Koolen Syndrome; Koolen-De Vries Syndrome; Microdeletion 17q21.31 Syndrome; Monosomy 17q21.31
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; *Chromosome Deletion; Chromosomes, Human, Pair 17; *Intellectual Disability
Frequency: 45
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Chromosome 17q21.31 Deletion Syndrome MeSH Supplementary Concept Data 2024