craniodiaphyseal dysplasia, autosomal dominant

Preferred Label : craniodiaphyseal dysplasia, autosomal dominant;

Origin ID

C567275;

UMLS CUI

C2675746;

Currated CISMeF NLP mapping
- Craniodiaphyseal dysplasia, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- craniofacial abnormalities [MeSH Descriptor]
- osteochondrodysplasias [MeSH Descriptor]
Record concept(s)
- craniodiaphyseal dysplasia, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniodiaphyseal dysplasia, autosomal dominant [OMIM Phenotype]