ONKI3 | Medical Subject Headings


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Porphyrias 34 coordinate concepts 2 subordinate concepts ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic ∟ Acid-Base Imbalance \| ∟ Amyloidosis \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Mitochondrial Diseases \| ∟ Phosphorus Metabolism Disorders \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance \| ∟ Lipodystrophy \| ∟ Necrobiosis Lipoidica \| ∟ 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 \| ∟ Progeria \| ∟ Purine-Pyrimidine Metabolism, Inborn Errors \| ∟ Renal Tubular Transport, Inborn Errors \| ∟ Steroid Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Porphyrias 34 coordinate concepts 2 subordinate concepts ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic ∟ Acid-Base Imbalance \| ∟ Amyloidosis \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Mitochondrial Diseases \| ∟ Phosphorus Metabolism Disorders \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance \| ∟ Lipodystrophy \| ∟ Necrobiosis Lipoidica \| ∟ 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 \| ∟ Progeria \| ∟ Purine-Pyrimidine Metabolism, Inborn Errors \| ∟ Renal Tubular Transport, Inborn Errors \| ∟ Steroid Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Porphyrias 34 coordinate concepts 2 subordinate concepts ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic ∟ Acid-Base Imbalance \| ∟ Amyloidosis \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Mitochondrial Diseases \| ∟ Phosphorus Metabolism Disorders \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance \| ∟ Lipodystrophy \| ∟ Necrobiosis Lipoidica \| ∟ 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 \| ∟ Progeria \| ∟ Purine-Pyrimidine Metabolism, Inborn Errors \| ∟ Renal Tubular Transport, Inborn Errors \| ∟ Steroid Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias 34 coordinate concepts 2 subordinate concepts ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic ∟ Acid-Base Imbalance \| ∟ Amyloidosis \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Mitochondrial Diseases \| ∟ Phosphorus Metabolism Disorders \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance \| ∟ Lipodystrophy \| ∟ Necrobiosis Lipoidica \| ∟ 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 \| ∟ Progeria \| ∟ Purine-Pyrimidine Metabolism, Inborn Errors \| ∟ Renal Tubular Transport, Inborn Errors \| ∟ Steroid Metabolism, Inborn Errors Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias 34 coordinate concepts 2 subordinate concepts ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic ∟ Acid-Base Imbalance \| ∟ Amyloidosis \| ∟ Brain Diseases, Metabolic \| ∟ Calcium Metabolism Disorders \| ∟ D008659Q000151* \| ∟ DNA Repair-Deficiency Disorders \| ∟ Glucose Metabolism Disorders \| ∟ Iron Metabolism Disorders \| ∟ Lipid Metabolism Disorders \| ∟ Malabsorption Syndromes \| ∟ Metabolic Syndrome X \| ∟ Metabolism, Inborn Errors \| ∟ Mitochondrial Diseases \| ∟ Phosphorus Metabolism Disorders \| ∟ Skin Diseases, Metabolic \| ∟ Wasting Syndrome \| ∟ Water-Electrolyte Imbalance \| ∟ Lipodystrophy \| ∟ Necrobiosis Lipoidica \| ∟ 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 \| ∟ Progeria \| ∟ Purine-Pyrimidine Metabolism, Inborn Errors \| ∟ 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 ∟ Porphyrias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Porphyrias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Porphyrias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias 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) Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Skin Diseases, Metabolic > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Skin Diseases, Metabolic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Porphyria, Erythropoietic \| Porphyrias, Hepatic X
Annotation:	general or unspecified: prefer specifics X
historyNote*:	2005 (1963) X
publicMeSHNote*:	2005; see PORPHYRIA 1963-2004 X
Scope note:	A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Related term:	Hydroxymethylbilane Synthase \| Porphobilinogen Synthase X
Type:	Concept X
Coordinate terms:	Acid-Base Imbalance \| Amyloidosis \| Brain Diseases, Metabolic \| Calcium Metabolism Disorders \| D008659Q000151* \| DNA Repair-Deficiency Disorders \| Glucose Metabolism Disorders \| Iron Metabolism Disorders \| Lipid Metabolism Disorders \| Malabsorption Syndromes \| Metabolic Syndrome X \| Metabolism, Inborn Errors \| Mitochondrial Diseases \| Phosphorus Metabolism Disorders \| Skin Diseases, Metabolic \| Wasting Syndrome \| Water-Electrolyte Imbalance \| Lipodystrophy \| Necrobiosis Lipoidica \| 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 \| Progeria \| Purine-Pyrimidine Metabolism, Inborn Errors \| Renal Tubular Transport, Inborn Errors \| Steroid Metabolism, Inborn Errors X
URI:	X
Labels and equivalent concepts:	Porfyriat (fi) Porfyria (fi, replaced) Porfyri (sv) Porphyria (en, replaced) Porphyria (la-FI, replaced) X
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