familial partial lipodystrophy, type 2

Preferred Label : familial partial lipodystrophy, type 2;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0487302;

UMLS CUI

C1720860;

Currated CISMeF NLP mapping
- Familial Partial Lipodystrophy Type 2 [NCIt concept]
- Familial partial lipodystrophy type 2 (disorder) [SNOMED CT concept]
- Familial partial lipodystrophy, Dunnigan type [ICD-11 More detail]
- Familial partial lipodystrophy, Dunnigan type [ORDO Disease]
- Lipodystrophy, familial partial, type 2 [OMIM Phenotype]
- familial partial lipodystrophy type 2 [DO Concept]
Related record
- lipodystrophy, familial partial [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Partial Lipodystrophy Type 2 [NCIt concept]
- Familial partial lipodystrophy type 2 (disorder) [SNOMED CT concept]
- Familial partial lipodystrophy, Dunnigan type [ORDO Disease]
- Lipodystrophy, familial partial, type 2 [OMIM Phenotype]
- familial partial lipodystrophy type 2 [DO Concept]