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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Schaaf-Yang syndrome
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Accession:DOID:0111715 term browser browse the term
Definition:A syndrome characterized by delayed psychomotor development, impaired intellectual development, hypotonia, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the maternally imprinted gene MAGEL2 on chromosome 15q11.2. (DO)
Synonyms:exact_synonym: Chitayat-Hall syndrome;   MAGEL2-RELATED CONDITION;   MAGEL2-related PWLS;   MAGEL2-related Prader-Willi-like syndrome;   PWLS;   Prader-Willi-like syndrome;   SHFYNG;   distal arthrogryposis with hypopituitarism, mental retardation, and facial anomalies
 primary_id: MESH:C535385
 alt_id: OMIM:615547
 xref: GARD:13316;   ORDO:398069

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Schaaf-Yang syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Magel2 MAGE family member L2 ISO ClinVar Annotator: match by term: MAGEL2-related condition | ClinVar Annotator: match by term: Schaaf-Yang syndrome OMIM
ClinVar		 PMID:24076603 PMID:24088041 PMID:25326635 PMID:25473036 PMID:25590979 More... NCBI chrNW_004955416:31,091,306...31,095,420
Ensembl chrNW_004955416:31,091,151...31,095,484 		JBrowse link
G Sim1 SIM bHLH transcription factor 1 ISO ClinVar Annotator: match by term: Schaaf-Yang syndrome ClinVar PMID:25741868 NCBI chrNW_004955411:26,173,009...26,256,545
Ensembl chrNW_004955411:26,173,009...26,259,752 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16063
    syndrome 9329
      Prader-Willi syndrome 16
        Schaaf-Yang syndrome 2
Path 2
Term Annotations click to browse term
  disease 16063
    disease of anatomical entity 13820
      nervous system disease 12088
        central nervous system disease 10855
          brain disease 10186
            disease of mental health 7327
              developmental disorder of mental health 4976
                specific developmental disorder 4103
                  intellectual disability 3919
                    Prader-Willi syndrome 16
                      Schaaf-Yang syndrome 2
paths to the root