MeSH Browser

MeSH Supplementary: Schaaf-Yang syndrome
Unique ID: C000726748
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000726748
Entry Term(s): Chitayat-Hall syndrome; Prader-Willi-like syndrome; SHFYNG
Registry Numbers: 0
Heading Mapped to: *Developmental Disabilities; *Hypopituitarism; *Facies; *Chromosome Disorders; *Imprinting Disorders
Note: autosomal dominant multisystem disorder characterized by delayed psychomotor development, impaired intellectual development, hypotonia, and behavioral abnormalities and associated with paternal mutations in the MAGEL2 gene.
Date of Entry: 2023/02/07
Revision Date: 2023/04/14

Concept UI: M000762633
Registry Numbers: 0
Terms: Schaaf-Yang syndrome Preferred Term
Term UI T001132668
Date02/07/2023
LexicalTag EPO
ThesaurusID NLM (2023); Prader-Willi-like syndrome
Term UI T001132670
Date02/07/2023
LexicalTag EPO
ThesaurusID NLM (2023); Chitayat-Hall syndrome
Term UI T001132671
Date02/07/2023
LexicalTag EPO
ThesaurusID NLM (2023); SHFYNG
Term UI T001132669
Date02/07/2023
LexicalTag NON
ThesaurusID NLM (2023)

Schaaf-Yang syndrome MeSH Supplementary Concept Data 2025