Glucosephosphate Dehydrogenase Deficiency [nedostatek glukóza-6-fosfátdehydrogenázy]

topical
15
Terms

deficience G6PD
deficience glukóza-6-fosfátdehydrogenázy
deficit G6PD
deficit glukosa-6-fosfátdehydrogenasy
deficit glukóza-6-fosfátdehydrogenázy
deficit glukózo-6-fosfát dehydrogenázy
glukosafosfátdehydrogenasa - nedostatek
nedostatek glukosa-6-fosfátdehydrogenasy
nedostatek glukózo-6-fosfátdehydrogenázy

 

Deficiency of Glucose-6-Phosphate Dehydrogenase
Deficiency, Glucosephosphate Dehydrogenase
Deficiency, GPD
G6PD Deficiency
Glucose 6 Phosphate Dehydrogenase Deficiency
Glucose-6-Phosphate Dehydrogenase Deficiency
Glucosephosphate Dehydrogenase Deficiencies
GPD Deficiency
Hemolytic Anemia Due to G6PD Deficiency

Persistent link   https://www.medvik.cz/link/D005955
Definition

A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.

DUI
D005955 MeSH Browser
CUI
M0009353
History note
64
Public note
64

Allowable subheadings

BL
blood 1
CF
cerebrospinal fluid
CI
chemically induced 1
CL
classification
CO
complications
DI
diagnosis 4
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 1
GE
genetics 3
HI
history
IM
immunology
ME
metabolism 1
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
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 977
C15.378.050 Anemia 1 257
C15.378.050.141 Anemia, Hemolytic 262
C15.378.050.141.150 Anemia, Hemolytic, Congenital 48
C15.378.050.141.150.095 Anemia, Dyserythropoietic, Congenital 16
C15.378.050.141.150.100 Anemia, Hemolytic, Congenital Nonspherocytic 13
C15.378.050.141.150.150 Anemia, Sickle Cell 45
C15.378.050.141.150.365 Elliptocytosis, Hereditary 6
C15.378.050.141.150.480 Glucosephosphate Dehydrogenase Deficiency 15
C15.378.050.141.150.480.370 Favism 6
C15.378.050.141.150.490 Hemoglobin C Disease 1
C15.378.050.141.150.785 Spherocytosis, Hereditary 43
C15.378.050.141.150.875 Thalassemia 87
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 219
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.070.095 Anemia, Dyserythropoietic, Congenital 16
C16.320.070.100 Anemia, Hemolytic, Congenital Nonspherocytic 13
C16.320.070.150 Anemia, Sickle Cell 45
C16.320.070.365 Elliptocytosis, Hereditary 6
C16.320.070.480 Glucosephosphate Dehydrogenase Deficiency 15
C16.320.070.480.370 Favism 6
C16.320.070.490 Hemoglobin C Disease 1
C16.320.070.785 Spherocytosis, Hereditary 43
C16.320.070.875 Thalassemia 87
C16.320.565 Metabolism, Inborn Errors 715
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors 36
C16.320.565.202.125 Congenital Disorders of Glycosylation 31
C16.320.565.202.251 Fructose Metabolism, Inborn Errors 5
C16.320.565.202.303 Fucosidosis 2
C16.320.565.202.355 Galactosemias 44
C16.320.565.202.402 Glucosephosphate Dehydrogenase Deficiency 15
C16.320.565.202.449 Glycogen Storage Disease 46
C16.320.565.202.460 Hyperoxaluria, Primary 10
C16.320.565.202.589 Lactose Intolerance 132
C16.320.565.202.607 Mannosidase Deficiency Diseases 1
C16.320.565.202.670 Mucolipidoses 10
C16.320.565.202.715 Mucopolysaccharidoses 81
C16.320.565.202.720 Multiple Carboxylase Deficiency
C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors 6
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 205
C18.452.648 Metabolism, Inborn Errors 715
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors 36
C18.452.648.202.125 Congenital Disorders of Glycosylation 31
C18.452.648.202.251 Fructose Metabolism, Inborn Errors 5
C18.452.648.202.303 Fucosidosis 2
C18.452.648.202.355 Galactosemias 44
C18.452.648.202.402 Glucosephosphate Dehydrogenase Deficiency 15
C18.452.648.202.449 Glycogen Storage Disease 46
C18.452.648.202.460 Hyperoxaluria, Primary 10
C18.452.648.202.589 Lactose Intolerance 132
C18.452.648.202.607 Mannosidase Deficiency Diseases 1
C18.452.648.202.670 Mucolipidoses 10
C18.452.648.202.715 Mucopolysaccharidoses 81
C18.452.648.202.720 Multiple Carboxylase Deficiency
C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors 6

Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency Disease MeSH Browser

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