Lipodystrophy, Congenital Generalized [kongenitální generalizovaná lipodystrofie]

topical
1
Terms

Berardinelliho syndrom
Berardinelliho-Seipův syndrom
Berardinelliův syndrom
Berardinelliův-Seipův syndrom
generalizovaná lipodystrofie
kongenitální generalizovaná lipodystrofie typ 1
kongenitální generalizovaná lipodystrofie typ 2
lipodystrofie kongenitální generalizovaná
lipodystrofie vrozená generalizovaná
Seipův syndrom

 

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

Persistent link   https://www.medvik.cz/link/D052497
Definition

Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.

DUI
D052497 MeSH Browser
CUI
M0487299
Previous indexing
Lipodystrophy (1968-2006)
History note
2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006
Public note
2007; see DIABETES MELLITUS, LIPOATROPHIC 2005-2006

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.565 Metabolism, Inborn Errors 711
C16.320.565.398 Lipid Metabolism, Inborn Errors 154
C16.320.565.398.224 Barth Syndrome 6
C16.320.565.398.450 Hyperlipidemia, Familial Combined 68
C16.320.565.398.465 Hyperlipoproteinemia Type I 21
C16.320.565.398.481 Hyperlipoproteinemia Type II 455
C16.320.565.398.483 Hyperlipoproteinemia Type III 19
C16.320.565.398.487 Hyperlipoproteinemia Type IV 14
C16.320.565.398.493 Hyperlipoproteinemia Type V 6
C16.320.565.398.500 Hypolipoproteinemias 35
C16.320.565.398.641 Lipidoses 35
C16.320.565.398.745 Lipodystrophy, Congenital Generalized 1
C16.320.565.398.850 Smith-Lemli-Opitz Syndrome 30
C16.320.565.398.925 Xanthomatosis, Cerebrotendinous
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 799
C17.800.849 Skin Diseases, Metabolic 17
C17.800.849.391 Lipodystrophy 37
C17.800.849.391.400 HIV-Associated Lipodystrophy Syndrome 5
C17.800.849.391.550 Lipodystrophy, Congenital Generalized 1
C17.800.849.391.700 Lipodystrophy, Familial Partial 1
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 196
C18.452.584 Lipid Metabolism Disorders 99
C18.452.584.563 Lipid Metabolism, Inborn Errors 154
C18.452.584.563.224 Barth Syndrome 6
C18.452.584.563.450 Hyperlipidemia, Familial Combined 68
C18.452.584.563.465 Hyperlipoproteinemia Type I 21
C18.452.584.563.481 Hyperlipoproteinemia Type II 455
C18.452.584.563.483 Hyperlipoproteinemia Type III 19
C18.452.584.563.487 Hyperlipoproteinemia Type IV 14
C18.452.584.563.493 Hyperlipoproteinemia Type V 6
C18.452.584.563.497 Hypobetalipoproteinemia, Familial, Apolipoprotein B 1
C18.452.584.563.500 Hypolipoproteinemias 35
C18.452.584.563.641 Lipidoses 35
C18.452.584.563.745 Lipodystrophy, Congenital Generalized 1
C18.452.584.563.798 Lipodystrophy, Familial Partial 1
C18.452.584.563.824 Shwachman-Diamond Syndrome 2
C18.452.584.563.850 Smith-Lemli-Opitz Syndrome 30
C18.452.584.563.925 Xanthomatosis, Cerebrotendinous
C18.452.584.625 Lipodystrophy 37
C18.452.584.625.400 HIV-Associated Lipodystrophy Syndrome 5
C18.452.584.625.550 Lipodystrophy, Congenital Generalized 1
C18.452.584.625.700 Lipodystrophy, Familial Partial 1
C18.452.648 Metabolism, Inborn Errors 711
C18.452.648.398 Lipid Metabolism, Inborn Errors 154
C18.452.648.398.224 Barth Syndrome 6
C18.452.648.398.450 Hyperlipidemia, Familial Combined 68
C18.452.648.398.465 Hyperlipoproteinemia Type I 21
C18.452.648.398.481 Hyperlipoproteinemia Type II 455
C18.452.648.398.483 Hyperlipoproteinemia Type III 19
C18.452.648.398.487 Hyperlipoproteinemia Type IV 14
C18.452.648.398.493 Hyperlipoproteinemia Type V 6
C18.452.648.398.500 Hypolipoproteinemias 35
C18.452.648.398.641 Lipidoses 35
C18.452.648.398.745 Lipodystrophy, Congenital Generalized 1
C18.452.648.398.850 Smith-Lemli-Opitz Syndrome 30
C18.452.648.398.925 Xanthomatosis, Cerebrotendinous
C18.452.880 Skin Diseases, Metabolic 17
C18.452.880.391 Lipodystrophy 37
C18.452.880.391.400 HIV-Associated Lipodystrophy Syndrome 5
C18.452.880.391.550 Lipodystrophy, Congenital Generalized 1
C18.452.880.391.700 Lipodystrophy, Familial Partial 1

Lipodystrophy, Congenital Generalized, Type 3 Disease MeSH Browser

Lipodystrophy, Congenital Generalized, Type 4 Disease MeSH Browser

Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones Disease MeSH Browser

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