Metal Metabolism, Inborn Errors [vrozené poruchy metabolismu kovů]

topical
16
Terms

kovy - vrozené poruchy metabolismu

 

Metal Metabolism, Inborn Error

Persistent link   https://www.medvik.cz/link/D008664
Definition

Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.

Annotation
coordinate with specific metal /metab
DUI
D008664 MeSH Browser
CUI
M0013499
History note
65
Public note
65

Allowable subheadings

BL
blood 1
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 2
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 3
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 1
GE
genetics 3
HI
history
IM
immunology
ME
metabolism 2
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 3
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
C16.320.565.151 Amino Acid Transport Disorders, Inborn 1
C16.320.565.176 Amyloidosis, Familial 16
C16.320.565.189 Brain Diseases, Metabolic, Inborn 26
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors 36
C16.320.565.240 Cytochrome-c Oxidase Deficiency 27
C16.320.565.300 Hyperbilirubinemia, Hereditary 35
C16.320.565.398 Lipid Metabolism, Inborn Errors 154
C16.320.565.595 Lysosomal Storage Diseases 72
C16.320.565.618 Metal Metabolism, Inborn Errors 16
C16.320.565.618.337 Hemochromatosis 198
C16.320.565.618.403 Hepatolenticular Degeneration 243
C16.320.565.618.482 Hypophosphatasia 16
C16.320.565.618.544 Hypophosphatemia, Familial 12
C16.320.565.618.590 Menkes Kinky Hair Syndrome 12
C16.320.565.618.711 Paralyses, Familial Periodic 7
C16.320.565.618.815 Pseudohypoparathyroidism 31
C16.320.565.663 Peroxisomal Disorders 20
C16.320.565.753 Progeria 27
C16.320.565.798 Purine-Pyrimidine Metabolism, Inborn Errors 40
C16.320.565.893 Renal Tubular Transport, Inborn Errors 36
C16.320.565.925 Steroid Metabolism, Inborn Errors 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
C18.452.648.151 Amino Acid Transport Disorders, Inborn 1
C18.452.648.176 Amyloidosis, Familial 16
C18.452.648.189 Brain Diseases, Metabolic, Inborn 26
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors 36
C18.452.648.300 Hyperbilirubinemia, Hereditary 35
C18.452.648.398 Lipid Metabolism, Inborn Errors 154
C18.452.648.595 Lysosomal Storage Diseases 72
C18.452.648.618 Metal Metabolism, Inborn Errors 16
C18.452.648.618.337 Hemochromatosis 198
C18.452.648.618.403 Hepatolenticular Degeneration 243
C18.452.648.618.482 Hypophosphatasia 16
C18.452.648.618.544 Hypophosphatemia, Familial 12
C18.452.648.618.590 Menkes Kinky Hair Syndrome 12
C18.452.648.618.711 Paralyses, Familial Periodic 7
C18.452.648.618.815 Pseudohypoparathyroidism 31
C18.452.648.663 Peroxisomal Disorders 20
C18.452.648.753 Progeria 27
C18.452.648.798 Purine-Pyrimidine Metabolism, Inborn Errors 40
C18.452.648.893 Renal Tubular Transport, Inborn Errors 36
C18.452.648.925 Steroid Metabolism, Inborn Errors 7

Congenital atransferrinemia Disease MeSH Browser

Copper Toxicosis, Idiopathic Disease MeSH Browser

Hyperzincemia with Functional Zinc Depletion Disease MeSH Browser

Molybdenum Cofactor Deficiency, Complementation Group A Disease MeSH Browser

Molybdenum Cofactor Deficiency, Complementation Group B Disease MeSH Browser

Molybdenum Cofactor Deficiency, Complementation Group C Disease MeSH Browser

Molybdenum cofactor deficiency Disease MeSH Browser

hyperzincemia and hypercalprotectinemia Disease MeSH Browser

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