Ornithine Carbamoyltransferase Deficiency Disease
"Ornithine Carbamoyltransferase Deficiency Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)
Descriptor ID |
D020163
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MeSH Number(s) |
C10.228.140.163.100.937.750 C16.320.322.828 C16.320.565.100.940.750 C16.320.565.189.937.750 C18.452.132.100.937.500 C18.452.648.100.940.500 C18.452.648.189.937.500
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Concept/Terms |
Ornithine Carbamoyltransferase Deficiency Disease- Ornithine Carbamoyltransferase Deficiency Disease
- Ornithine Transcarbamylase Deficiency Disease
- Deficiency Disease, Ornithine Transcarbamylase
- Ornithine Transcarbamylase Deficiency
- Deficiencies, Ornithine Transcarbamylase
- Deficiency, Ornithine Transcarbamylase
- Ornithine Transcarbamylase Deficiencies
- OTC Deficiency
- Deficiencies, OTC
- Deficiency, OTC
- OTC Deficiencies
- Deficiency Disease, Ornithine Carbamoyltransferase
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Below are MeSH descriptors whose meaning is more general than "Ornithine Carbamoyltransferase Deficiency Disease".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Urea Cycle Disorders, Inborn [C10.228.140.163.100.937]
- Ornithine Carbamoyltransferase Deficiency Disease [C10.228.140.163.100.937.750]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Ornithine Carbamoyltransferase Deficiency Disease [C16.320.322.828]
- Metabolism, Inborn Errors [C16.320.565]
- Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
- Urea Cycle Disorders, Inborn [C16.320.565.100.940]
- Ornithine Carbamoyltransferase Deficiency Disease [C16.320.565.100.940.750]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Urea Cycle Disorders, Inborn [C16.320.565.189.937]
- Ornithine Carbamoyltransferase Deficiency Disease [C16.320.565.189.937.750]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Urea Cycle Disorders, Inborn [C18.452.132.100.937]
- Ornithine Carbamoyltransferase Deficiency Disease [C18.452.132.100.937.500]
- Metabolism, Inborn Errors [C18.452.648]
- Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
- Urea Cycle Disorders, Inborn [C18.452.648.100.940]
- Ornithine Carbamoyltransferase Deficiency Disease [C18.452.648.100.940.500]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Urea Cycle Disorders, Inborn [C18.452.648.189.937]
- Ornithine Carbamoyltransferase Deficiency Disease [C18.452.648.189.937.500]
Below are MeSH descriptors whose meaning is more specific than "Ornithine Carbamoyltransferase Deficiency Disease".
This graph shows the total number of publications written about "Ornithine Carbamoyltransferase Deficiency Disease" by people in this website by year, and whether "Ornithine Carbamoyltransferase Deficiency Disease" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1984 | 0 | 1 | 1 | 1986 | 1 | 0 | 1 | 1998 | 0 | 1 | 1 | 2011 | 1 | 0 | 1 |
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Below are the most recent publications written about "Ornithine Carbamoyltransferase Deficiency Disease" by people in Profiles.
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Lipskind S, Loanzon S, Simi E, Ouyang DW. Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids. J Perinatol. 2011 Oct; 31(10):682-4.
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Whitington PF, Alonso EM, Boyle JT, Molleston JP, Rosenthal P, Emond JC, Millis JM. Liver transplantation for the treatment of urea cycle disorders. J Inherit Metab Dis. 1998; 21 Suppl 1:112-8.
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Batshaw ML, Msall M, Beaudet AL, Trojak J. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency. J Pediatr. 1986 Feb; 108(2):236-41.
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Msall M, Batshaw ML, Suss R, Brusilow SW, Mellits ED. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies. N Engl J Med. 1984 Jun 07; 310(23):1500-5.
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