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
|
| 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
|
| Concept/Terms |
Ornithine Carbamoyltransferase Deficiency Disease- Ornithine Carbamoyltransferase Deficiency Disease
- Ornithine Carbamoyltransferase Deficiency
- Ornithine Transcarbamylase Deficiency Disease
- Deficiency Disease, Ornithine Carbamoyltransferase
- Deficiency Disease, Ornithine Transcarbamylase
- Ornithine Transcarbamylase Deficiency
- Deficiencies, Ornithine Transcarbamylase
- Deficiency, Ornithine Transcarbamylase
- Ornithine Transcarbamylase Deficiencies
- Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To
- OTC Deficiency
- Deficiencies, OTC
- Deficiency, OTC
- OTC Deficiencies
|
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".
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