Peroxisomal D-bifunctional enzyme deficiency (Q88702): Difference between revisions
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Refere ao distúrbio de oxidação de ácidos graxos peroxissomais autossômicos recessivos. Os distúrbios peroxissomais são geralmente causados por uma combinação de defeitos de montagem peroxissomal ou por deficiências de enzimas peroxissômicas específicas. | |||
| description / en | description / en | ||
This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes. | |||
Revision as of 15:05, 15 August 2026
This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_996981847 |
||
| English | Peroxisomal D-bifunctional enzyme deficiency |
This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes. |
