progeria syndrome, Childhood-Onset

Preferred Label : progeria syndrome, Childhood-Onset;

MeSH note : promote to HM;

Origin ID

C567661;

UMLS CUI

C2750285;

Automatic exact mappings (from CISMeF team)
- Hutchinson-gilford progeria syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- progeria [MeSH Descriptor]
Record concept(s)
- progeria syndrome, Childhood-Onset [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]