Lipoatrophic Diabetes Mellitus

Preferred Label : Lipoatrophic Diabetes Mellitus;

NCIt definition : A rare syndrome characterized by almost complete absence of body fat, accentuated muscularity, insulin-resistant diabetes, hyperlipidemia, hepatomegaly, and hypermetabolism.;

Details

Origin ID

C34537;

UMLS CUI

C0011859;

Automatic exact mappings (from CISMeF team)
- Berardinelli-Seip congenital lipodystrophy [ICD-11 More detail]
- Lipoatrophic diabetes [MedDRA LLT]
- Lipoatrophic diabetes [PASCAL descriptor]
- lipoatrophic diabetes mellitus [DO Concept]
CISMeF manual mappings
- Lipoatrophic diabetes (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Congenital total lipodystrophy (disorder) [SNOMED CT concept]
- diabetes mellitus, lipoatrophic [MeSH Descriptor]
- diabetes mellitus, lipoatrophic [MeSH concept]
- lipoatrophic diabetes mellitus [Disease (Nov.)]
- lipodystrophy, nos [SNOMED Notion]
DO Cross reference
- lipoatrophic diabetes mellitus [DO Concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Pancreas [NCIt concept]
See also inter- (CISMeF)
- Congenital generalized lipodystrophy [ORDO Disease]
- congenital generalized lipodystrophy [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lipoatrophic diabetes [MedDRA LLT]
- Lipoatrophic diabetes (disorder) [SNOMED CT concept]
- diabetes mellitus, lipoatrophic [MeSH Descriptor]
- diabetes mellitus, lipoatrophic [MeSH concept]
- lipoatrophic diabetes mellitus [DO Concept]
- lipoatrophic diabetes mellitus [Disease (Nov.)]
disease_has_normal_cell_origin
- Islet Cell [NCIt concept]
disease_has_normal_tissue_origin
- Islet of Langerhans [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Islet of Langerhans [NCIt concept]

Keyword's position in hierarchy(ies) :

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