lipodystrophy, nos

Preferred Label : lipodystrophy, nos;

Détails

Origin ID

DB-61700;

UMLS CUI

C0023787;

Automatic exact mappings (from CISMeF team)
- Berardinelli-Seip congenital lipodystrophy [ICD-11 More detail]
- Lipoatrophic diabetes [PASCAL descriptor]
- Lipoatrophic diabetes [MedDRA LLT]
- Lipodystrophy absent (situation) [SNOMED CT concept]
- Lipodystrophy, not elsewhere classified [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Congenital total lipodystrophy (disorder) [SNOMED CT concept]
- LIPODYSTROPHY [WHO-ART Preferred Term]
- Lipoatrophic Diabetes Mellitus [NCIt concept]
- Lipoatrophic diabetes (disorder) [SNOMED CT concept]
- Lipodystrophies [MedDRA High Level Term]
- Lipodystrophy [NCIt concept]
- Lipodystrophy [PASCAL descriptor]
- Lipodystrophy [HPO term]
- Lipodystrophy [MedDRA LLT]
- Lipodystrophy (disorder) [SNOMED CT concept]
- diabetes mellitus, lipoatrophic [MeSH concept]
- diabetes mellitus, lipoatrophic [MeSH Descriptor]
- lipodystrophy [MeSH Descriptor]
- lipodystrophy [MeSH concept]
- lipodystrophy, congenital generalized [MeSH Descriptor]
ICD-10 exact mapping(s)
- Lipodystrophy, not elsewhere classified [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Acquired lipodystrophy [ORDO Disease]
- Genetic lipodystrophy [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Progeroid syndrome [ORDO Disease]
- Rare endocrine disease [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Lipodystrophy (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- LIPODYSTROPHY [WHO-ART Preferred Term]
- Lipodystrophies [MedDRA High Level Term]
- Lipodystrophy [ICD-9 code]
- Lipodystrophy [NCIt concept]
- Lipodystrophy [HPO term]
- Lipodystrophy [PASCAL descriptor]
- Lipodystrophy [MedDRA LLT]
- Lipodystrophy (disorder) [SNOMED CT concept]
- lipodystrophy [MeSH concept]
- lipodystrophy [Disease (Nov.)]
- lipodystrophy [DO Concept]
- lipodystrophy [MeSH Descriptor]
Validated automatic mappings to BTNT
- Congenital generalized lipodystrophy [ORDO Disease]
- congenital generalized lipodystrophy [Disease (Nov.)]
- lipoatrophic diabetes mellitus [Disease (Nov.)]

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