progeroid syndrome, congenital, petty type

Preferred Label : progeroid syndrome, congenital, petty type;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0567660;

UMLS CUI

C2676780;

Automatic exact mappings (from CISMeF team)
- Progeroid syndrome Petty type (disorder) [SNOMED CT concept]
- Progeroid syndrome, Petty type [ORDO Disease]
Currated CISMeF NLP mapping
- Fontaine progeroid syndrome [OMIM Phenotype]
Related record
- progeroid syndrome, congenital, petty type [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fontaine progeroid syndrome [OMIM Phenotype]
- Gorlin-Chaudhry-Moss syndrome (disorder) [SNOMED CT concept]
- Progeroid syndrome Petty type (disorder) [SNOMED CT concept]