ONKI3 | Medical Subject Headings

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The way concept relations are shown: separately in hierarchy

Purine-Pyrimidine Metabolism, Inborn Errors

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Purine-Pyrimidine Metabolism, Inborn Errors 15 coordinate concepts 2 subordinate concepts ∟ Gout \| ∟ Lesch-Nyhan Syndrome ∟ Amino Acid Metabolism, Inborn Errors \| ∟ Amino Acid Transport Disorders, Inborn \| ∟ Amyloidosis, Familial \| ∟ Brain Diseases, Metabolic, Inborn \| ∟ Carbohydrate Metabolism, Inborn Errors \| ∟ Cytochrome-c Oxidase Deficiency \| ∟ Hyperbilirubinemia, Hereditary \| ∟ Lipid Metabolism, Inborn Errors \| ∟ Lysosomal Storage Diseases \| ∟ Metal Metabolism, Inborn Errors \| ∟ Peroxisomal Disorders \| ∟ Porphyrias \| ∟ Progeria \| ∟ Renal Tubular Transport, Inborn Errors \| ∟ Steroid Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Purine-Pyrimidine Metabolism, Inborn Errors 15 coordinate concepts 2 subordinate concepts ∟ Gout \| ∟ Lesch-Nyhan Syndrome ∟ Amino Acid Metabolism, Inborn Errors \| ∟ Amino Acid Transport Disorders, Inborn \| ∟ Amyloidosis, Familial \| ∟ Brain Diseases, Metabolic, Inborn \| ∟ Carbohydrate Metabolism, Inborn Errors \| ∟ Cytochrome-c Oxidase Deficiency \| ∟ Hyperbilirubinemia, Hereditary \| ∟ Lipid Metabolism, Inborn Errors \| ∟ Lysosomal Storage Diseases \| ∟ Metal Metabolism, Inborn Errors \| ∟ Peroxisomal Disorders \| ∟ Porphyrias \| ∟ Progeria \| ∟ Renal Tubular Transport, Inborn Errors \| ∟ Steroid Metabolism, Inborn Errors X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Purine-Pyrimidine Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Purine-Pyrimidine Metabolism, Inborn Errors Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Gout \| Lesch-Nyhan Syndrome X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; coord IM with specific purine /metab (IM) or pyrimidine /metab (IM); DF: PP METAB INBORN ERR X
historyNote*:	65 X
publicMeSHNote*:	65 X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Amino Acid Metabolism, Inborn Errors \| Amino Acid Transport Disorders, Inborn \| Amyloidosis, Familial \| Brain Diseases, Metabolic, Inborn \| Carbohydrate Metabolism, Inborn Errors \| Cytochrome-c Oxidase Deficiency \| Hyperbilirubinemia, Hereditary \| Lipid Metabolism, Inborn Errors \| Lysosomal Storage Diseases \| Metal Metabolism, Inborn Errors \| Peroxisomal Disorders \| Porphyrias \| Progeria \| Renal Tubular Transport, Inborn Errors \| Steroid Metabolism, Inborn Errors X
URI:	X
Labels and equivalent concepts:	Synnynnäiset puriini-pyrimidiiniaineenvaihdunnan häiriöt (fi) Synnynnäiset puriini-pyrimidiinimetabolian häiriöt (fi, replaced) Puriini-pyrimidiinimetabolian synnynnäiset häiriöt (fi, replaced) Puriini-pyrimidiiniaineenvaihdunnan synnynnäiset häiriöt (fi, replaced) Purin-pyrimidin, medfödda ämnesomsättningsrubbningar (sv) Purine Pyrimidine Metabolism, Inborn Errors (en, replaced) X
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