familial generalized lipodystrophy - CISMeF

" /> familial generalized lipodystrophy - CISMeF

CISMeF

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Familial generalized lipodystrophySNOMED Notion

Preferred Label : familial generalized lipodystrophy;

Details

Origin ID

DB-61710;

UMLS CUI

C0221032;

Automatic exact mappings (from CISMeF team)
- Acquired generalized lipodystrophy [ORDO Disease]
- Acquired generalized lipodystrophy (disorder) [SNOMED CT concept]
- Berardinelli lipodystrophy [PASCAL descriptor]
- Congenital lipoatrophic diabetes [MedDRA LLT]
- Congenital lipodystrophy [MedDRA LLT]
- Generalised lipodystrophy [MedDRA LLT]
- Generalized lipodystrophy [MedDRA LLT]
- Generalized lipodystrophy [HPO term]
- Lipodystrophy congenital [MedDRA LLT]
CISMeF manual mappings
- Congenital total lipodystrophy (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Berardinelli-Seip Congenital Lipodystrophy [NCIt concept]
- Berardinelli-Seip syndrome [MedDRA LLT]
- Congenital generalised lipodystrophy [MedDRA Preferred Term]
- Congenital generalised lipodystrophy [ICD-11 Sub-sub category]
- Congenital generalized lipodystrophy [HPO term]
- Congenital generalized lipodystrophy [MedDRA LLT]
- Congenital generalized lipodystrophy [ORDO Disease]
- Familial generalized lipodystrophy (disorder) [Inactive SNOMED CT concept]
- Lipodystrophy, congenital generalized [OMIM phenotypic series]
- congenital generalized lipodystrophy [Disease (Nov.)]
- congenital generalized lipodystrophy [DO Concept]
- diabetes mellitus, lipoatrophic [MeSH Descriptor]
- lipodystrophy, congenital generalized [MeSH concept]
- lipodystrophy, congenital generalized [MeSH Descriptor]
ICD-10 exact mapping(s)
- Lipodystrophy, not elsewhere classified [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Acquired lipodystrophy [ORDO Disease]
- Genetic lipodystrophy [ORDO Disease]
- Progeroid syndrome [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
See also inter- (CISMeF)
- lipoatrophic diabetes mellitus [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Berardinelli-Seip Congenital Lipodystrophy [NCIt concept]
- Berardinelli-Seip syndrome [MedDRA LLT]
- Congenital generalised lipodystrophy [MedDRA Preferred Term]
- Congenital generalised lipodystrophy [ICD-11 Sub-sub category]
- Congenital generalized lipodystrophy [MedDRA LLT]
- Congenital generalized lipodystrophy [HPO term]
- Congenital generalized lipodystrophy [ORDO Disease]
- Congenital lipoatrophic diabetes [MedDRA LLT]
- Congenital lipodystrophy [MedDRA LLT]
- Congenital total lipoatrophy (disorder) [Inactive SNOMED CT concept]
- Congenital total lipodystrophy (disorder) [SNOMED CT concept]
- Familial generalized lipodystrophy (disorder) [Inactive SNOMED CT concept]
- Generalized lipodystrophy [HPO term]
- Lawrence-Seip syndrome [MedDRA LLT]
- Lipodystrophy congenital [MedDRA LLT]
- Total lipodystrophy [MedDRA LLT]
- congenital generalized lipodystrophy [Disease (Nov.)]
- congenital generalized lipodystrophy [DO Concept]
- congenital lipodystrophy [Disease (Nov.)]
- lipodystrophy, congenital generalized [MeSH Descriptor]
- lipodystrophy, congenital generalized [MeSH concept]

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01/05/2025

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