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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Ornithine Carbamoyltransferase Deficiency Disease
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Urea Cycle Disorders, Inborn > Ornithine Carbamoyltransferase Deficiency Disease
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Urea Cycle Disorders, Inborn > Ornithine Carbamoyltransferase Deficiency Disease
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Urea Cycle Disorders, Inborn > Ornithine Carbamoyltransferase Deficiency Disease
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Urea Cycle Disorders, Inborn > Ornithine Carbamoyltransferase Deficiency Disease
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Urea Cycle Disorders, Inborn > Ornithine Carbamoyltransferase Deficiency Disease
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Urea Cycle Disorders, Inborn > Ornithine Carbamoyltransferase Deficiency Disease

Preferred term

Ornithine Carbamoyltransferase Deficiency Disease  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Deficiencies, Ornithine Transcarbamylase
  • Deficiencies, OTC
  • Deficiency Disease, Ornithine Carbamoyltransferase
  • Deficiency Disease, Ornithine Transcarbamylase
  • Deficiency, Ornithine Transcarbamylase
  • Deficiency, OTC
  • Ornithine Carbamoyltransferase Deficiency
  • Ornithine Transcarbamylase Deficiencies
  • Ornithine Transcarbamylase Deficiency
  • Ornithine Transcarbamylase Deficiency Disease
  • Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To
  • OTC Deficiencies
  • OTC Deficiency

Scope note

  • 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)

History note

  • 2000

In other languages

URI

http://www.yso.fi/onto/mesh/D020163

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