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Metal Metabolism, Inborn Errors
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Metal Metabolism, Inborn Errors
Tree Number(s)
C16.320.565.618
C18.452.648.618
Unique ID
D008664
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D008664
Annotation
coordinate with specific metal
/metab
Scope Note
Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.
Entry Version
METAL METAB INBORN ERR
Entry Term(s)
Metal Metabolism, Inborn Error
Public MeSH Note
65
History Note
65
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
2016/07/07
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Amino Acid Transport Disorders, Inborn [C16.320.565.151]
Amyloidosis, Familial [C16.320.565.176]
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
Cytochrome-c Oxidase Deficiency [C16.320.565.240]
Hyperbilirubinemia, Hereditary [C16.320.565.300]
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Lysosomal Storage Diseases [C16.320.565.595]
Metal Metabolism, Inborn Errors [C16.320.565.618]
Hemochromatosis [C16.320.565.618.337]
Hepatolenticular Degeneration [C16.320.565.618.403]
Hypophosphatasia [C16.320.565.618.482]
Hypophosphatemia, Familial [C16.320.565.618.544]
Menkes Kinky Hair Syndrome [C16.320.565.618.590]
Paralyses, Familial Periodic [C16.320.565.618.711]
Pseudohypoparathyroidism [C16.320.565.618.815]
Peroxisomal Disorders [C16.320.565.663]
Progeria [C16.320.565.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C16.320.565.798]
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Steroid Metabolism, Inborn Errors [C16.320.565.925]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
Amino Acid Transport Disorders, Inborn [C18.452.648.151]
Amyloidosis, Familial [C18.452.648.176]
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
Hyperbilirubinemia, Hereditary [C18.452.648.300]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Lysosomal Storage Diseases [C18.452.648.595]
Metal Metabolism, Inborn Errors [C18.452.648.618]
Hemochromatosis [C18.452.648.618.337]
Hepatolenticular Degeneration [C18.452.648.618.403]
Hypophosphatasia [C18.452.648.618.482]
Hypophosphatemia, Familial [C18.452.648.618.544]
Menkes Kinky Hair Syndrome [C18.452.648.618.590]
Paralyses, Familial Periodic [C18.452.648.618.711]
Pseudohypoparathyroidism [C18.452.648.618.815]
Peroxisomal Disorders [C18.452.648.663]
Progeria [C18.452.648.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C18.452.648.798]
Renal Tubular Transport, Inborn Errors [C18.452.648.893]
Steroid Metabolism, Inborn Errors [C18.452.648.925]
Expand All
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Metal Metabolism, Inborn Errors
Preferred
Concept UI
M0013499
Scope Note
Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero.
Terms
Metal Metabolism, Inborn Errors
Preferred Term
Term UI
T025767
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1965)
Metal Metabolism, Inborn Error
Term UI
T025766
Date
05/24/1990
LexicalTag
NON
ThesaurusID
NLM (1991)
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