progeria syndrome

Preferred Label : progeria syndrome;

Origin ID

D4-00401;

UMLS CUI

C0033300;

Automatic exact mappings (from CISMeF team)
- Progeria [ICD-11 More detail]
- cockayne syndrome [MeSH Descriptor]
Currated CISMeF NLP mapping
- Hutchinson-Gilford progeria syndrome [ORDO Disease]
- Hutchinson-Gilford syndrome (disorder) [SNOMED CT concept]
- Hutchinson-gilford progeria syndrome [OMIM Phenotype]
- Progeria [NCIt concept]
- Progeria [PASCAL descriptor]
- Progeria [MedDRA Preferred Term]
- progeria [Disease (Nov.)]
- progeria [DO Concept]
- progeria [MeSH Descriptor]
- progeria [MeSH concept]
False UMLS correspondences (reviewed by CISMeF team)
- Hutchinson-Gilford syndrome (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other specified endocrine disorders [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Ectodermal malformation syndrome associated with ocular features [ORDO Disease]
- Nuclear cell envelopathy [ORDO Disease]
- Primary osteolysis [ORDO Disease]
- Progeroid syndrome [ORDO Disease]
- Rare developmental defect with skin/mucosae involvement [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hutchinson-Gilford progeria syndrome [ORDO Disease]
- Hutchinson-gilford progeria syndrome [OMIM Phenotype]
- Progeria [PASCAL descriptor]
- Progeria [NCIt concept]
- Progeria [MedDRA Preferred Term]
- progeria [MeSH Descriptor]
- progeria [MeSH concept]
- progeria [Disease (Nov.)]
- progeria [DO Concept]