familial lipodystrophy of limbs and trunk

Preferred Label : familial lipodystrophy of limbs and trunk;

Details

Origin ID

DB-61730;

UMLS CUI

C0271694;

Currated CISMeF NLP mapping
- Familial Partial Lipodystrophy [NCIt concept]
- Familial partial lipodystrophy [ICD-11 More detail]
- Familial partial lipodystrophy [MedDRA Preferred Term]
- Familial partial lipodystrophy [ORDO Disease]
- Familial partial lipodystrophy (disorder) [SNOMED CT concept]
- Lipodystrophy, familial partial [OMIM phenotypic series]
- familial partial lipodystrophy [Disease (Nov.)]
- familial partial lipodystrophy [DO Concept]
- lipodystrophy, familial partial [MeSH Descriptor]
- lipodystrophy, familial partial [MeSH concept]
ICD-10 exact mapping(s)
- Lipodystrophy, not elsewhere classified [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- AKT2-related familial partial lipodystrophy [ORDO Disease]
- Mandibuloacral dysplasia [ORDO Disease]
- PPARG-related familial partial lipodystrophy [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Genetic lipodystrophy [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Familial partial lipodystrophy (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Partial Lipodystrophy [NCIt concept]
- Familial partial lipodystrophy [ORDO Disease]
- Familial partial lipodystrophy [MedDRA Preferred Term]
- Familial partial lipodystrophy (disorder) [SNOMED CT concept]
- familial partial lipodystrophy [Disease (Nov.)]
- familial partial lipodystrophy [DO Concept]
- lipodystrophy, familial partial [MeSH concept]
- lipodystrophy, familial partial [MeSH Descriptor]

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