Multiple Acyl Coenzyme A Dehydrogenase Deficiency [mnohočetný deficit acyl-CoA dehydrogenáz]

topical
2
Terms

acyl-CoA-dehydrogenasa - mnohočetná deficience
acyl-CoA-dehydrogenasa - mnohočetný deficit
glutarová acidurie II. typu
glutarová acidurie IIA
glutarová acidurie IIB
glutarová acidurie IIC
glutarová acidurie typu II
mnohočetný deficit acyl-CoA dehydrogenázy

 

Electron Transfer Flavoprotein Alpha Subunit Deficiency
Electron Transfer Flavoprotein Beta Subunit Deficiency
Electron Transfer Flavoprotein Deficiency
Electron Transfer Flavoprotein Dehydrogenase Deficiency
ETFA Deficiency
ETFB Deficiency
ETFDH Deficiency
Ethylmalonic-Adipic Aciduria
Ethylmalonic-Adipicaciduria
Glutaric Acidemia Type II
Glutaric Acidemia, Type 2
Glutaric Aciduria II
Glutaric Aciduria IIA
Glutaric Aciduria IIB
Glutaric Aciduria IIC
Glutaric Aciduria Type 2
Glutaric Aciduria Type II
Glutaric Aciduria, Type 2
MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)
Multiple Acyl-CoA Dehydrogenase Deficiency
Multiple FAD Dehydrogenase Deficiency

Persistent link   https://www.medvik.cz/link/D054069
Definition

An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1).

DUI
D054069 MeSH Browser
CUI
M0500981
History note
2008
Public note
2008

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 1
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 1
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 1
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
C16.320.565.100 Amino Acid Metabolism, Inborn Errors 124
C16.320.565.100.102 Albinism 17
C16.320.565.100.187 Alkaptonuria 76
C16.320.565.100.477 Hyperglycinemia, Nonketotic 7
C16.320.565.100.480 Hyperhomocysteinemia 212
C16.320.565.100.544 Hyperlysinemias
C16.320.565.100.608 Maple Syrup Urine Disease 8
C16.320.565.100.614 Multiple Acyl Coenzyme A Dehydrogenase Deficiency 2
C16.320.565.100.620 Multiple Carboxylase Deficiency
C16.320.565.100.766 Phenylketonurias 285
C16.320.565.100.794 Prolidase Deficiency
C16.320.565.100.823 Propionic Acidemia 3
C16.320.565.100.880 Tyrosinemias 18
C16.320.565.100.940 Urea Cycle Disorders, Inborn 7
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 196
C18.452.648 Metabolism, Inborn Errors 711
C18.452.648.100 Amino Acid Metabolism, Inborn Errors 124
C18.452.648.100.102 Albinism 17
C18.452.648.100.187 Alkaptonuria 76
C18.452.648.100.477 Hyperglycinemia, Nonketotic 7
C18.452.648.100.480 Hyperhomocysteinemia 212
C18.452.648.100.544 Hyperlysinemias
C18.452.648.100.608 Maple Syrup Urine Disease 8
C18.452.648.100.614 Multiple Acyl Coenzyme A Dehydrogenase Deficiency 2
C18.452.648.100.620 Multiple Carboxylase Deficiency
C18.452.648.100.766 Phenylketonurias 285
C18.452.648.100.823 Propionic Acidemia 3
C18.452.648.100.880 Tyrosinemias 18
C18.452.648.100.940 Urea Cycle Disorders, Inborn 7
C18.452.660 Mitochondrial Diseases 159
C18.452.660.097 Carbamoyl-Phosphate Synthase I Deficiency Disease 1
C18.452.660.195 Cytochrome-c Oxidase Deficiency 27
C18.452.660.300 Friedreich Ataxia 54
C18.452.660.520 Leigh Disease 26
C18.452.660.560 Mitochondrial Myopathies 40
C18.452.660.612 Multiple Acyl Coenzyme A Dehydrogenase Deficiency 2
C18.452.660.665 Optic Atrophy, Autosomal Dominant 3
C18.452.660.670 Optic Atrophy, Hereditary, Leber 24
C18.452.660.705 Pyruvate Carboxylase Deficiency Disease
C18.452.660.710 Pyruvate Dehydrogenase Complex Deficiency Disease 9

Glutaric aciduria 2 Disease MeSH Browser

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