Genee-Wiedemann syndrome

Preferred Label : Genee-Wiedemann syndrome;

CISMeF acronym : GWAFD;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0532141;

UMLS CUI

C0265257;

Currated CISMeF NLP mapping
- Miller syndrome [Disease (Nov.)]
- Miller syndrome [OMIM Phenotype]
- Miller syndrome (disorder) [SNOMED CT concept]
- Postaxial acrofacial dysostosis [ORDO Disease]
- miller syndrome [SNOMED Notion]
Related record
- Genee-Wiedemann syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Miller syndrome [OMIM Phenotype]
- Miller syndrome [Disease (Nov.)]
- Miller syndrome (disorder) [SNOMED CT concept]
- Postaxial acrofacial dysostosis [ORDO Disease]
- miller syndrome [SNOMED Notion]
- postaxial acrofacial dysostosis [DO Concept]