ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Porphyria, Acute Intermittent

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Liver Diseases ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent 5 coordinate concepts ∟ Coproporphyria, Hereditary \| ∟ Porphyria Cutanea Tarda \| ∟ Porphyria, Hepatoerythropoietic \| ∟ Porphyria, Variegate \| ∟ Protoporphyria, Erythropoietic X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Liver Diseases ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Metabolic ∟ Porphyrias ∟ Porphyrias, Hepatic ∟ Porphyria, Acute Intermittent Porphyrias, Hepatic > Porphyrias > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Liver Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Porphyrias > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Porphyrias > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Porphyrias > Skin Diseases, Metabolic > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Porphyrias, Hepatic > Porphyrias > Skin Diseases, Metabolic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
History note:	Porphyria (1966-1992)X
historyNote*:	93 X
publicMeSHNote*:	93 X
Scope note:	An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features are recurrent and life-threatening neurologic disturbances, ABDOMINAL PAIN, and elevated level of AMINOLEVULINIC ACID and PORPHOBILINOGEN in the urine. X
activeMeSHYear*:	2007X
dateCreated*:	1992-05-22X
dateEstablished*:	1993-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	PXPX
Type:	Concept X
Coordinate terms:	Coproporphyria, Hereditary \| Porphyria Cutanea Tarda \| Porphyria, Hepatoerythropoietic \| Porphyria, Variegate \| Protoporphyria, Erythropoietic X
URI:	X
Labels and equivalent concepts:	Akuutti intermittoiva porfyria (fi) Porfyria, akuutti intermittoiva (fi, replaced) Äkillinen intermittoiva porfyria (fi, replaced) Porfyri, akut intermittent (sv) Acute Porphyria (en, replaced) Porphyria intermittens acuta (la-FI, replaced) Porphyria acuta intermittens (la-FI, replaced) X
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