MeSH Browser

MeSH Heading: Lipodystrophy, Congenital Generalized
Tree Number(s): C16.320.565.398.745; C17.800.849.391.550; C18.452.584.563.745; C18.452.584.625.550; C18.452.648.398.745; C18.452.880.391.550
Unique ID: D052497
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D052497
Scope Note: Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.
Entry Term(s): Berardinelli Syndrome; Berardinelli-Seip Congenital Lipodystrophy; Berardinelli-Seip Congenital Lipodystrophy Type 1; Berardinelli-Seip Congenital Lipodystrophy Type 2; Berardinelli-Seip Congenital Lipodystrophy, Type 1; Berardinelli-Seip Congenital Lipodystrophy, Type 2; Berardinelli-Seip Syndrome; Brunzell Syndrome; Brunzell Syndrome (with Bone Cysts); Brunzell Syndrome, AGPAT2-Related; Brunzell Syndrome, BSCL2-Related; Congenital Generalized Lipodystrophy; Congenital Generalized Lipodystrophy Type 1; Congenital Generalized Lipodystrophy Type 2; Congenital Lipoatrophic Diabetes; Generalized Lipodystrophy; Lipoatrophic Diabetes, Congenital; Lipodystrophy, Berardinelli-Seip Congenital, Type 1; Lipodystrophy, Berardinelli-Seip Congenital, Type 2; Lipodystrophy, Congenital Generalized, Type 1; Lipodystrophy, Congenital Generalized, Type 2; Lipodystrophy, Total, And Acromegaloid Gigantism; Seip Syndrome; Total Lipodystrophy; Total Lipodystrophy and Acromegaloid Gigantism
Previous Indexing: Lipodystrophy (1968-2006)
Public MeSH Note: 2007; see DIABETES MELLITUS, LIPOATROPHIC 2005-2006
History Note: 2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2021/06/30

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]
    - Lipid Metabolism, Inborn Errors [C16.320.565.398]

Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
  - Skin Diseases, Metabolic [C17.800.849]
    - Lipodystrophy [C17.800.849.391]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Lipid Metabolism Disorders [C18.452.584]
    - Lipid Metabolism, Inborn Errors [C18.452.584.563]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Lipid Metabolism Disorders [C18.452.584]
    - Lipodystrophy [C18.452.584.625]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Lipid Metabolism, Inborn Errors [C18.452.648.398]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Skin Diseases, Metabolic [C18.452.880]
    - Lipodystrophy [C18.452.880.391]

Lipodystrophy, Congenital Generalized Preferred

Congenital Generalized Lipodystrophy Type 1 Narrower

Congenital Generalized Lipodystrophy Type 2 Narrower

Lipodystrophy, Congenital Generalized MeSH Descriptor Data 2023