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| Descriptor en español: |
Errores Innatos del Metabolismo de los Aminoácidos
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| Descriptor en inglés: | Amino Acid Metabolism, Inborn Errors | ||||||
| Descriptor en portugués: | Erros Inatos do Metabolismo dos Aminoácidos | ||||||
| Descriptor en francés: | Aminoacidopathies congénitales | ||||||
| Término(s) alternativo(s): |
Amino Acid Metabolism Disorders, Inborn Amino Acid Metabolism, Inborn Error Amino Acid Metabolism, Inherited Disorders Amino Acidopathies, Congenital Amino Acidopathies, Inborn Amino Acidopathy, Congenital Amino Acidopathy, Inborn Congenital Amino Acidopathies Congenital Amino Acidopathy Inborn Amino Acidopathies Inborn Amino Acidopathy Inborn Errors, Amino Acid Metabolism Inherited Errors of Amino Acid Metabolism |
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| Código(s) jeráquico(s): |
C16.320.565.100 C18.452.648.100 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D000592 | ||||||
| Nota de alcance: | Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (e.g., ACIDOSIS) and neurologic manifestations. They are present at birth, although they may not become symptomatic until later in life. |
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| Nota de indización: | coord IM with specific amino acid /metab (IM) |
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| Calificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Nota Pública de MeSH: | 1965; PROTEIN METABOLISM DISORDERS was heading 1963-1964 |
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| Nota de historia: | 1965; PROTEIN METABOLISM DISORDERS was heading 1963-1964 |
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| Versión alternativa: | AA METAB INBORN ERR |
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| Identificador de DeCS: | 596 | ||||||
| ID del Descriptor: | D000592 | ||||||
| Clasificación de la NLM: | WD 205.5.A5 | ||||||
| Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
| Fecha de establecimiento: | 01/01/1965 | ||||||
| Fecha de entrada: | 01/01/1999 | ||||||
| Fecha de revisión: | 05/07/2006 |
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Amino Acid Metabolism, Inborn Errors
- Concepto preferido
Amino Acid Metabolism, Inherited Disorders
- Más estrecho
| UI del concepto |
M0000918 |
| Nota de alcance | Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (e.g., ACIDOSIS) and neurologic manifestations. They are present at birth, although they may not become symptomatic until later in life. |
| Término preferido | Amino Acid Metabolism, Inborn Errors |
| Término(s) alternativo(s) |
Amino Acid Metabolism Disorders, Inborn Amino Acid Metabolism, Inborn Error Amino Acidopathies, Congenital Amino Acidopathies, Inborn Amino Acidopathy, Congenital Amino Acidopathy, Inborn Congenital Amino Acidopathies Congenital Amino Acidopathy Inborn Amino Acidopathies Inborn Amino Acidopathy Inborn Errors, Amino Acid Metabolism |
| UI del concepto |
M0333991 |
| Término preferido | Amino Acid Metabolism, Inherited Disorders |
| Término(s) alternativo(s) |
Inherited Errors of Amino Acid Metabolism |
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