MeSH Browser

MeSH Supplementary: Emanuel syndrome
Unique ID: C535733
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535733
Entry Term(s): Der(22) Syndrome Due To 3:1 Meiotic Disjunction Events; Supernumary Der(22) Syndrome; Supernumary Der(22)T(11;22) Syndrome; Supernumary Derivative 22 Chromosome Syndrome; Supernumerary der(22) syndrome; Supernumerary der(22)t(11;22) syndrome
Registry Numbers: 0
Heading Mapped to: *Cleft Palate; *Heart Defects, Congenital; *Intellectual Disability; *Muscle Hypotonia; *Chromosome Disorders
Frequency: 21
Note: Caused by a t(11;22)(q23;q11.2) translocation.
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Emanuel syndrome MeSH Supplementary Concept Data 2024