Malignant hyperphenylalaninaemia due to tetrahydrobiopterin deficiency (Q93272): Difference between revisions
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Condição caracterizada por níveis moderadamente ou fortemente elevados do aminoácido fenilalanina no sangue. Esse diagnóstico se deve a um raro distúrbio metabólico que aumenta os níveis sanguíneos de fenilalanina. | |||
| description / en | description / en | ||
This condition is characterised by mildly or strongly elevated levels of the amino acid phenylalanine in the blood. This diagnosis is due to a rare metabolic disorder that increases the blood levels of phenylalanine. | |||
Revision as of 08:22, 16 August 2026
This condition is characterised by mildly or strongly elevated levels of the amino acid phenylalanine in the blood. This diagnosis is due to a rare metabolic disorder that increases the blood levels of phenylalanine.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1659163210 |
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| English | Malignant hyperphenylalaninaemia due to tetrahydrobiopterin deficiency |
This condition is characterised by mildly or strongly elevated levels of the amino acid phenylalanine in the blood. This diagnosis is due to a rare metabolic disorder that increases the blood levels of phenylalanine. |
