| Descriptor English: | Pyruvate Metabolism, Inborn Errors | ||||||
| Descriptor Spanish: |
Errores Innatos del Metabolismo del Piruvato
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| Descriptor Portuguese: | Erros Inatos do Metabolismo dos Piruvatos | ||||||
| Descriptor French: | Erreurs innées du métabolisme du pyruvate | ||||||
| Tree number(s): |
C16.320.565.202.810 C18.452.648.202.810 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015323 | ||||||
| Scope note: | Hereditary disorders of pyruvate metabolism. They are difficult to diagnose and describe because pyruvate is a key intermediate in glycolysis, gluconeogenesis, and the tricarboxylic acid cycle. Some inherited metabolic disorders may alter pyruvate metabolism indirectly. Disorders in pyruvate metabolism appear to lead to deficiencies in neurotransmitter synthesis and, consequently, to nervous system disorders. |
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| Allowable Qualifiers: |
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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| Previous Indexing: |
Carbohydrate Metabolism, Inborn Errors (1966-1988) Pyruvates (1966-1988) |
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| Public MeSH Note: | 89 |
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| History Note: | 89 |
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| Entry Version: | PYRUVATE METAB INBORN ERR |
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| DeCS ID: | 23809 | ||||||
| Unique ID: | D015323 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1989/01/01 | ||||||
| Date of Entry: | 1988/05/31 | ||||||
| Revision Date: | 2006/07/05 |
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Pyruvate Metabolism, Inborn Errors
- Preferred
| Concept UI |
M0023592 |
| Scope note | Hereditary disorders of pyruvate metabolism. They are difficult to diagnose and describe because pyruvate is a key intermediate in glycolysis, gluconeogenesis, and the tricarboxylic acid cycle. Some inherited metabolic disorders may alter pyruvate metabolism indirectly. Disorders in pyruvate metabolism appear to lead to deficiencies in neurotransmitter synthesis and, consequently, to nervous system disorders. |
| Preferred term | Pyruvate Metabolism, Inborn Errors |
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