Fragile Site 16p12 MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Fragile Site 16p12
Unique ID: C565001
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565001
Registry Number: 0
Heading Mapped to: Mental Disorders; Developmental Disabilities; *Chromosome Deletion; Chromosomes, Human, Pair 16; *Heart Defects, Congenital; *Craniofacial Abnormalities; *Chromosome Disorders
Frequency: 3
Note: deletion = Chromomsome 16p12.1 Deletion Syndrome
Date of Entry: 2012/11/05

Fragile Site 16p12 Preferred

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