MeSH Browser

MeSH Supplementary: Chromosome 3q29 Deletion Syndrome
Unique ID: C567184
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567184
Entry Term(s): Microdeletion 3q29 Syndrome
Registry Numbers: 0
Heading Mapped to: Developmental Disabilities; *Chromosome Deletion; Chromosomes, Human, Pair 3; *Intellectual Disability
Frequency: 16
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome 3q29 Deletion Syndrome MeSH Supplementary Concept Data 2025