Ehlers-Danlos syndrome, autosomal dominant, type unspecified

Preferred Label : Ehlers-Danlos syndrome, autosomal dominant, type unspecified;

MeSH synonym : Ehlers-Danlos syndrome, Friedman-Harrod type;

Origin ID

C562424;

UMLS CUI

C0220679;

Currated CISMeF NLP mapping
- Classical Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-danlos syndrome, autosomal dominant, type unspecified [OMIM Phenotype]
MeSH term(s) associated for indexing
- ehlers-danlos syndrome [MeSH Descriptor]
Record concept(s)
- Ehlers-Danlos syndrome, autosomal dominant, type unspecified [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Classical Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-danlos syndrome, autosomal dominant, type unspecified [OMIM Phenotype]