Schaaf-Yang syndrome

Preferred Label : Schaaf-Yang syndrome;

MeSH synonym : Chitayat-Hall syndrome; SHFYNG; Prader-Willi-like syndrome;

Origin ID

C000726748;

UMLS CUI

C5575066;

Currated CISMeF NLP mapping
- Prader-Willi-like syndrome [ORDO Disease]
- Prader-Willi-like syndrome (disorder) [SNOMED CT concept]
- Schaaf-Yang syndrome [DO Concept]
- Schaaf-yang syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- Imprinting Disorders [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- developmental disabilities [MeSH Descriptor]
- facies [MeSH Descriptor]
- hypopituitarism [MeSH Descriptor]
Record concept(s)
- Schaaf-Yang syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- MAGE family member L2-related Prader-Willi-like syndrome (disorder) [SNOMED CT concept]
- Schaaf-yang syndrome [OMIM Phenotype]
Validated automatic mappings to BTNT
- MAGEL2-related Prader-Willi-like syndrome [ORDO Disease]