rett syndrome, atypical

Preferred Label : rett syndrome, atypical;

Origin ID

C567576;

UMLS CUI

C2748910;

Automatic exact mappings (from CISMeF team)
- Atypical Rett syndrome [ICD-11 More detail]
- Rett syndrome [OMIM Phenotype]
Currated CISMeF NLP mapping
- Atypical Rett syndrome [ORDO Disease]
- Atypical Rett syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- rett syndrome [MeSH Descriptor]
Record concept(s)
- rett syndrome, atypical [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atypical Rett syndrome [ORDO Disease]
- Atypical Rett syndrome (disorder) [SNOMED CT concept]