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Emanuel syndrome MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
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