MeSH Browser

MeSH Supplementary: Young Simpson syndrome
Unique ID: C536717
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536717
Entry Term(s): Blepharophimosis and Mental Retardation Syndrome, Say-Barber-Biesecker-Young-Simpson Type; Blepharophimosis-Intellectual Deficit Syndrome, Say-Barber-Biesecker-Young-Simpson Type; Mental retardation unusual facies hypothyroidism; Ohdo Syndrome, SBBYS Variant; Ohdo Syndrome, Say-Barber-Biesecker Variant; Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant; SBBYS Variant of Ohdo Syndrome; Say-Barber-Biesecker-Young-Simpson Syndrome; Say-Barber-Biesecker-Young-Simpson Variant of Ohdo Syndrome; Young-Simpson Syndrome
Heading Mapped to: *Congenital Hypothyroidism; *Heart Defects, Congenital; *Joint Instability; *Intellectual Disability; *Blepharophimosis; *Facies
Frequency: 21
Note: Sbbyss; Bmrs Sbbys not included
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Young Simpson syndrome MeSH Supplementary Concept Data 2024