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Propionic acidemia, also known as propionic aciduria or propionyl-CoA carboxylase deficiency (PCC deficiency), is a rare autosomal recessive metabolic disorder, classified as a branched-chain organic acidemia.
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propionic acidemia propionyl-coa symptoms enzyme acids disorder also acid poor valine methionine isoleucine threonine vomiting lethargy muscle citation needed carboxylase
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Propionic acidemia | Diagnostic method | Genetic testing; high levels of propionic acid in the urine | 1.00 | infobox |
| Propionic acidemia | Other names | Hyperglycinemia with ketoacidosis and leukopenia | 1.00 | infobox |
| Propionic acidemia | Prognosis | Development may be normal, or patients may have lifelong learning disabilities | 1.00 | infobox |
| Propionic acidemia | Specialty | Endocrinology | 1.00 | infobox |
| Propionic acidemia | Symptoms | Poor muscle tone, lethargy, vomiting | 1.00 | infobox |
| Propionic acidemia | Treatment | Low-protein diet | 1.00 | infobox |
| walking or talking | instance of | cause seizures and delays to normal development | 0.80 | text |
| Propionic acidemia | related to Epidemiology | Propionic | 0.60 | section |
| Propionic acidemia | related to Epidemiology | United States | 0.60 | section |
| Propionic acidemia | related to Epidemiology | The | 0.60 | section |
| Propionic acidemia | related to Epidemiology | Saudi Arabia | 0.60 | section |
| Propionic acidemia | related to Epidemiology | Amish | 0.60 | section |
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