Lipidoses [lipidózy]

topical
35
Terms

lipidóza
lipoidóza

 

Lipidosis
Lipoidosis

Persistent link   https://www.medvik.cz/link/D008064
Definition

Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.

Annotation
general or unspecified; prefer specifics
DUI
D008064 MeSH Browser
CUI
M0012566
History note
2007 (1966)
Public note
2007; see LIPOIDOSIS 1966-2006

Allowable subheadings

BL
blood 2
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 5
CO
complications 2
DI
diagnosis 7
DG
diagnostic imaging
DH
diet therapy 1
DT
drug therapy 2
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology 1
EH
ethnology
ET
etiology 3
GE
genetics
HI
history
IM
immunology
ME
metabolism 5
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 6
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 3
UR
urine
VE
veterinary 2
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 214
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 456
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
C16.320.565.398.641.201 Cholesterol Ester Storage Disease 13
C16.320.565.398.641.509 Neuronal Ceroid-Lipofuscinoses 29
C16.320.565.398.641.723 Sjogren-Larsson Syndrome 4
C16.320.565.398.641.803 Sphingolipidoses 12
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
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 197
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 456
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
C18.452.584.563.641.201 Cholesterol Ester Storage Disease 13
C18.452.584.563.641.509 Neuronal Ceroid-Lipofuscinoses 29
C18.452.584.563.641.723 Sjogren-Larsson Syndrome 4
C18.452.584.563.641.803 Sphingolipidoses 12
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
C18.452.648 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 456
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
C18.452.648.398.641.201 Cholesterol Ester Storage Disease 13
C18.452.648.398.641.509 Neuronal Ceroid-Lipofuscinoses 29
C18.452.648.398.641.723 Sjogren-Larsson Syndrome 4
C18.452.648.398.641.803 Sphingolipidoses 12
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

Cardiac Lipidosis, Familial Disease MeSH Browser

Cephalin Lipidosis Disease MeSH Browser

Neurovisceral Storage Disease with Curvilinear Bodies Disease MeSH Browser

Tremor of Intention, Ataxia, and Lipofuscinosis Disease MeSH Browser

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