ONKI3 | Medical Subject Headings

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia 5 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Chondrodysplasia Punctata, Rhizomelic \| ∟ Refsum Disease \| ∟ Refsum Disease, Infantile \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Peroxisomal Disorders ∟ Acatalasia 5 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Chondrodysplasia Punctata, Rhizomelic \| ∟ Refsum Disease \| ∟ Refsum Disease, Infantile \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia 5 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Chondrodysplasia Punctata, Rhizomelic \| ∟ Refsum Disease \| ∟ Refsum Disease, Infantile \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia 5 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Chondrodysplasia Punctata, Rhizomelic \| ∟ Refsum Disease \| ∟ Refsum Disease, Infantile \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia 5 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Chondrodysplasia Punctata, Rhizomelic \| ∟ Refsum Disease \| ∟ Refsum Disease, Infantile \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Peroxisomal Disorders ∟ Acatalasia 5 coordinate concepts ∟ Adrenoleukodystrophy \| ∟ Chondrodysplasia Punctata, Rhizomelic \| ∟ Refsum Disease \| ∟ Refsum Disease, Infantile \| ∟ Zellweger Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Peroxisomal Disorders ∟ Acatalasia Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Brain Diseases, Metabolic ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Brain Diseases, Metabolic, Inborn ∟ Peroxisomal Disorders ∟ Acatalasia Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Peroxisomal Disorders ∟ Acatalasia Peroxisomal Disorders > Brain Diseases, Metabolic, Inborn > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Peroxisomal Disorders > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Peroxisomal Disorders > Brain Diseases, Metabolic, Inborn > Brain Diseases, Metabolic > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Peroxisomal Disorders > Brain Diseases, Metabolic, Inborn > Brain Diseases, Metabolic > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Peroxisomal Disorders > Brain Diseases, Metabolic, Inborn > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Peroxisomal Disorders > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
History note:	Catalase (1965-1999)X
historyNote*:	2000 X
publicMeSHNote*:	2000 X
Scope note:	A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present. X
activeMeSHYear*:	2007X
dateCreated*:	1999-11-03X
dateEstablished*:	2000-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	adpX
Type:	Concept X
Coordinate terms:	Adrenoleukodystrophy \| Chondrodysplasia Punctata, Rhizomelic \| Refsum Disease \| Refsum Disease, Infantile \| Zellweger Syndrome X
URI:	X
Labels and equivalent concepts:	Akatalasia (fi) Takaharan sairaus (fi, replaced) Takaharan tauti (fi, replaced) Katalaasin puutos (fi, replaced) Katalaasin puute (fi, replaced) Akatalasemi (sv) Hypocatalasia (en, replaced) Takahara Disease (en, replaced) Takahara's Disease (en, replaced) Acatalasemia (en, replaced) Acatalasia (la-FI, replaced) Morbus Takahara (la-FI, replaced) X
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